11278 Mono-axial Screw
| Product No. | Dia. | Length |
| 11278-(030-055) | 5.0 | 30-55 |
| 11124-(135-147) | 5.5 | 35/37.5/40/42.5/45/47.5 |
| 11124-(022-032) | 6.0 | 50/52.5/55/57.5/60/62.5/65/70 |
11279 Poly-axial Screw
| Product No. | Dia | Length |
| 11125-(012-018) | 3.5 | 12/14/16/18 |
11280 Fixing Rod IV (φ5.5)
| Product No. | Dia | Length |
| 11125-(112-118) | 3.5 | 12/14/16/18 |
11281 Fixing Rod IV（φ5.5）
| Product No. | Dia | Length |
| 11126-(012-018) | 2.5 | 12/14/16/18 |
11282 Break-off Setscrew
| Product No. | Dia | Length |
| 11126-(012-018) | 2.5 | 12/14/16/18 |
The Master 7-LLA Spinal System is engineered to provide rigid posterior fixation of the thoracic, lumbar, and sacral spine, offering precision, strength, and flexibility for a wide range of spinal pathologies.
Reduced implant profile to minimize soft tissue disruption and postoperative discomfort.
Anatomically contoured rods and tulip heads designed to fit patient anatomy and optimize construct alignment.
Polyaxial screws with a wide angulation range (typically ±25°–30°) for ease of placement and rod capture.
Monoaxial screws available for specific trauma or deformity correction needs.
Cannulated screws compatible with minimally invasive techniques and guidewire-assisted insertion.
Available in multiple diameters and lengths for precise pedicle targeting.
Dual-lead screw thread with a reliable locking cap or set screw system ensures secure rod capture and prevents loosening.
Anti-cross-threading design enhances ease of insertion and safety.
Rod diameters typically ranging from 5.5 mm to 6.0 mm, in titanium or CoCr (cobalt-chrome) materials.
Compatible with pre-bent and intraoperatively bendable rods for optimal spinal contouring.
Full range of crosslinks, lateral connectors, domino connectors, and reduction screws.
Facilitates complex reconstructions, deformity corrections, and revision procedures.
Ergonomic, color-coded instruments with quick-connect features.
Designed for open and MIS (minimally invasive) techniques.
Instruments allow for power-assisted insertion, reduction, and compression/distraction maneuvers.
Implants made of Ti6Al4V ELI titanium alloy (ASTM F136) and CoCr.
Radiolucency maintained for intraoperative fluoroscopy with clear visualization of landmarks.
Designed for use in conditions like degenerative disc disease, spinal deformities (e.g., scoliosis, kyphosis), trauma, spondylolisthesis, and tumor reconstruction.
Also compatible with osteoporotic bone screw options for enhanced fixation.
Defined as back pain of discogenic origin with degeneration confirmed by imaging and clinical symptoms.
Narrowing of the spinal canal leading to nerve compression and neurological symptoms.
Includes isthmic and degenerative types (Grade I and II) causing vertebral instability.
Traumatic instability in the thoracolumbar spine requiring stabilization.
Such as scoliosis, kyphosis, and lordosis requiring correction and support.
For patients with failed previous spinal fusion (pseudoarthrosis) or implant failure requiring replacement or reinforcement.
Used to stabilize the spine after removal of pathological tissue.
Such as osteomyelitis or discitis, when accompanied by spinal instability requiring fixation.
Intended to be used in conjunction with bone graft (autograft or allograft) to facilitate posterior spinal fusion.
Intended for use in the thoracic (T1–T12), lumbar (L1–L5), and sacral (S1–S2) regions of the spine.
locking copmression plate brochure.pdf
The WALEN system is used in anterior cervical discectomy and fusion (ACDF) procedures to treat conditions such as degenerative disc disease, herniated discs, cervical spondylosis, and instability between C2–T1 vertebrae.
It is a zero-profile or low-profile integrated interbody device with anterior screw fixation. It may include titanium or PEEK cage options, depending on the model.
It is typically indicated for one or two adjacent cervical levels (e.g., C3–C4, C5–C6). Some models may support up to three levels depending on regulatory approvals and surgeon assessment.
Titanium alloy (Ti-6Al-4V) – for plate and screw components, or full implants in some versions.
PEEK (polyether ether ketone) – an option for radiolucent cages with embedded radiographic markers.
The WALEN system offers both:
Fixed-angle screws for rigid stability.
Variable-angle screws (typically up to 15°–20°) to accommodate patient anatomy and facilitate optimal placement.
Yes. It features an anti-backout locking mechanism to prevent screw loosening after implantation, enhancing long-term construct stability.
The WALEN cage includes a central graft window and is compatible with:
Autograft (preferred)
Allograft
Synthetic bone graft substitutes (as per surgeon preference and hospital protocol)
Multiple heights, footprints, and lordotic angles (typically 6°, 8°, or 12°) are available to restore cervical alignment and accommodate patient anatomy.
Yes, the system is indicated for revision procedures such as pseudoarthrosis or hardware failure from previous ACDF surgeries.
Yes. All components are made from non-ferromagnetic materials, making the system MRI-conditional. Always verify with the specific product IFU for MRI safety labeling.
The WALEN Anterior Cervical System is:
FDA 510(k) cleared (U.S.)
CE marked (Europe), where applicable
May have additional regional registrations depending on market
11278 Mono-axial Screw
| Product No. | Dia. | Length |
| 11278-(030-055) | 5.0 | 30-55 |
| 11124-(135-147) | 5.5 | 35/37.5/40/42.5/45/47.5 |
| 11124-(022-032) | 6.0 | 50/52.5/55/57.5/60/62.5/65/70 |
11279 Poly-axial Screw
| Product No. | Dia | Length |
| 11125-(012-018) | 3.5 | 12/14/16/18 |
11280 Fixing Rod IV (φ5.5)
| Product No. | Dia | Length |
| 11125-(112-118) | 3.5 | 12/14/16/18 |
11281 Fixing Rod IV（φ5.5）
| Product No. | Dia | Length |
| 11126-(012-018) | 2.5 | 12/14/16/18 |
11282 Break-off Setscrew
| Product No. | Dia | Length |
| 11126-(012-018) | 2.5 | 12/14/16/18 |
The Master 7-LLA Spinal System is engineered to provide rigid posterior fixation of the thoracic, lumbar, and sacral spine, offering precision, strength, and flexibility for a wide range of spinal pathologies.
Reduced implant profile to minimize soft tissue disruption and postoperative discomfort.
Anatomically contoured rods and tulip heads designed to fit patient anatomy and optimize construct alignment.
Polyaxial screws with a wide angulation range (typically ±25°–30°) for ease of placement and rod capture.
Monoaxial screws available for specific trauma or deformity correction needs.
Cannulated screws compatible with minimally invasive techniques and guidewire-assisted insertion.
Available in multiple diameters and lengths for precise pedicle targeting.
Dual-lead screw thread with a reliable locking cap or set screw system ensures secure rod capture and prevents loosening.
Anti-cross-threading design enhances ease of insertion and safety.
Rod diameters typically ranging from 5.5 mm to 6.0 mm, in titanium or CoCr (cobalt-chrome) materials.
Compatible with pre-bent and intraoperatively bendable rods for optimal spinal contouring.
Full range of crosslinks, lateral connectors, domino connectors, and reduction screws.
Facilitates complex reconstructions, deformity corrections, and revision procedures.
Ergonomic, color-coded instruments with quick-connect features.
Designed for open and MIS (minimally invasive) techniques.
Instruments allow for power-assisted insertion, reduction, and compression/distraction maneuvers.
Implants made of Ti6Al4V ELI titanium alloy (ASTM F136) and CoCr.
Radiolucency maintained for intraoperative fluoroscopy with clear visualization of landmarks.
Designed for use in conditions like degenerative disc disease, spinal deformities (e.g., scoliosis, kyphosis), trauma, spondylolisthesis, and tumor reconstruction.
Also compatible with osteoporotic bone screw options for enhanced fixation.
Defined as back pain of discogenic origin with degeneration confirmed by imaging and clinical symptoms.
Narrowing of the spinal canal leading to nerve compression and neurological symptoms.
Includes isthmic and degenerative types (Grade I and II) causing vertebral instability.
Traumatic instability in the thoracolumbar spine requiring stabilization.
Such as scoliosis, kyphosis, and lordosis requiring correction and support.
For patients with failed previous spinal fusion (pseudoarthrosis) or implant failure requiring replacement or reinforcement.
Used to stabilize the spine after removal of pathological tissue.
Such as osteomyelitis or discitis, when accompanied by spinal instability requiring fixation.
Intended to be used in conjunction with bone graft (autograft or allograft) to facilitate posterior spinal fusion.
Intended for use in the thoracic (T1–T12), lumbar (L1–L5), and sacral (S1–S2) regions of the spine.
locking copmression plate brochure.pdf
The WALEN system is used in anterior cervical discectomy and fusion (ACDF) procedures to treat conditions such as degenerative disc disease, herniated discs, cervical spondylosis, and instability between C2–T1 vertebrae.
It is a zero-profile or low-profile integrated interbody device with anterior screw fixation. It may include titanium or PEEK cage options, depending on the model.
It is typically indicated for one or two adjacent cervical levels (e.g., C3–C4, C5–C6). Some models may support up to three levels depending on regulatory approvals and surgeon assessment.
Titanium alloy (Ti-6Al-4V) – for plate and screw components, or full implants in some versions.
PEEK (polyether ether ketone) – an option for radiolucent cages with embedded radiographic markers.
The WALEN system offers both:
Fixed-angle screws for rigid stability.
Variable-angle screws (typically up to 15°–20°) to accommodate patient anatomy and facilitate optimal placement.
Yes. It features an anti-backout locking mechanism to prevent screw loosening after implantation, enhancing long-term construct stability.
The WALEN cage includes a central graft window and is compatible with:
Autograft (preferred)
Allograft
Synthetic bone graft substitutes (as per surgeon preference and hospital protocol)
Multiple heights, footprints, and lordotic angles (typically 6°, 8°, or 12°) are available to restore cervical alignment and accommodate patient anatomy.
Yes, the system is indicated for revision procedures such as pseudoarthrosis or hardware failure from previous ACDF surgeries.
Yes. All components are made from non-ferromagnetic materials, making the system MRI-conditional. Always verify with the specific product IFU for MRI safety labeling.
The WALEN Anterior Cervical System is:
FDA 510(k) cleared (U.S.)
CE marked (Europe), where applicable
May have additional regional registrations depending on market
