Exceed™ Biplanar Expandable Interbody System
Exceed Biplanar is an expandable titanium-alloy lumbar interbody implant. It is supplied unexpanded, with a nose tapered in both lateral and vertical planes, and is expanded in place using…
Exceed Biplanar is an expandable titanium-alloy lumbar interbody implant. It is supplied unexpanded, with a nose tapered in both lateral and vertical planes, and is expanded in place using the system’s inserter.
The implant accommodates bone graft and has microscopic roughness with micro- and nanoscale features on its upper and lower surfaces. That surface is designed to resist migration at the vertebral interface.
Listed Item
25 mm (L) x 10 mm (W) x 13 mm (H), Lordotic 15°
Implant Configurations
Heights, lengths and lordotic angles vary across the range. The device is intended for one or two contiguous levels from L2 to S1 with autograft or specified allograft and supplemental fixation. Expansion and graft support are separate roles within the fusion construct.
Who Else Makes It
Concentrated in Jiangsu (6), Shandong (2), Shanghai (2). 7 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Apex (Guangzhou) Tools & Orthopedics Company | Guangzhou | Guangdong | Contract manufacturer | 62 |
| Paragon Medical Device (Changzhou) Co., Ltd. | Changzhou | Jiangsu | Contract manufacturer | 53 |
| Shandong Weigao Orthopaedic Device Co., Ltd. | Weihai | Shandong | Contract manufacturer | 42 |
| Suzhou Ahno Medical Devices Co., Ltd. | Suzhou | Jiangsu | Contract manufacturer | 17 |
| Zibo Dante Co., Ltd. | Zibo | Shandong | Contract manufacturer | 17 |
| Jiangsu Ideal Medical Science & Technology Co., Ltd. | Zhangjiagang | Jiangsu | Contract manufacturer | 7 |
| Zhisu Health Tech Jiaxing Co., Ltd. | Tongxiang | Zhejiang | Contract manufacturer | 4 |
| Medtronic (Changzhou) Medical Devices Technology Co., Ltd. | Changzhou | Jiangsu | Manufacturer | 53 |
| Shanghai Reach Medical Instrument Co., Ltd. | Shanghai | Shanghai | Manufacturer | 30 |
| Changzhou Geasure Medical Apparatus AND Instruments Co., Ltd. | Changzhou | Jiangsu | Contract manufacturer | 25 |
| Double Medical Technology Inc. | Xiamen | Fujian | Contract manufacturer | 14 |
| Zhejiang Decans Medical Devices Co., Ltd. | Jiaxing | Zhejiang | Manufacturer | 10 |
Showing 12 of 14. All 14 manufacturers in China registered for Intervertebral Fusion Device With Bone Graft, Lumbar
Record
| Listed by | Spine Wave, Inc., United States |
|---|---|
| FDA product code | MAX |
| Device type | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Device class | Class 2 |
| Regulation | 21 CFR 888.3080 |
| Establishment | Specification developer, Repacker / relabeller, Manufacturer |
| 510(k) | K231275 |
| Record published | 2023-12-11 |
| Record revised | 2025-07-14 (version 2) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Sterilisation | Moist Heat or Steam Sterilization |
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Label carries | lot or batch number, expiry date |
| Sizes | Length 22 to 25 mm; width 10 mm; height 9 to 14 mm; angle 0 to 15 ° |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 11-5341 | Length 22 mm | In distribution |
| 11-5351 | Length 25 mm | In distribution |
| 11-5332 | Length 25 mm | In distribution |
| 11-5339 | Length 22 mm | In distribution |
| 11-5331 | Length 25 mm | In distribution |
| 11-5354 | Length 22 mm | In distribution |
| 11-5434 | Length 25 mm | In distribution |
| 11-5343 | Length 22 mm | In distribution |
| 11-5334 | Length 25 mm | In distribution |
| 11-5349 | Length 25 mm | In distribution |
| 11-5333 | Length 25 mm | In distribution |
| 11-5417 | Length 22 mm | In distribution |
| 11-5340 | Length 22 mm | In distribution |
| 11-5355 | Length 22 mm | In distribution |
| 11-5348 | Length 25 mm | In distribution |
| 11-5357 | Length 22 mm | In distribution |
| 11-5433 | Length 25 mm | In distribution |
| 11-5335 | Length 25 mm | In distribution |
| 11-5430 | Length 25 mm | In distribution |
| 10-7701 | In distribution | |
| 10-7700 | In distribution | |
| 11-5336 | Length 25 mm | In distribution |
| 10-7706 | In distribution | |
| 11-5350 | Length 25 mm | In distribution |
| 11-5356 | Length 22 mm | In distribution |
| 11-5344 | Length 22 mm | In distribution |
| 10-7702 | In distribution | |
| 11-5415 | Length 22 mm | In distribution |
| 11-5412 | Length 22 mm | In distribution |
| 11-5342 | Length 22 mm | In distribution |
| 10-7707 | In distribution | |
| 11-5435 | Length 25 mm | In distribution |
| 11-5416 | Length 22 mm | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Peridot Intervertebral body fusion system | Gbs Commonwealth Co., Ltd. | 10,850 |
| Yellowstone | Summit Spine | 6,654 |
| CoRoent | Nuvasive, Inc. | 5,690 |
| Zavation | Zavation | 2,554 |
| Anyplus II Spinal Fixation System | GS Medical Co., Ltd. | 2,533 |
| Talos® IBF | Meditech Spine, LLC | 2,163 |
| Peridot-PT Intervertebral body fusion system | Gbs Commonwealth Co., Ltd. | 1,956 |
| TirboLOX-L Lumbar Ibfd | Captiva Spine, Inc. | 1,926 |
| Endoskeleton® TL | Titan Spine, LLC | 1,896 |
| Evos Lumbar Interbody System | Cutting Edge Spine | 1,871 |
| Epiphany | Pantheon Spinal LLC | 1,507 |
| LnK Lumbar Interbody Fusion Cage System | L&K Biomed Co., Ltd. | 1,506 |
Showing 12 of 1,958. All products under Intervertebral Fusion Device With Bone Graft, Lumbar
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K261159 | 2026-05-29 |
| K243816 | 2025-06-27 |
| K231275 | 2023-07-25 |
| K163246 | 2017-04-06 |
| K153222 | 2016-04-15 |
| K152620 | 2016-01-15 |
| K151581 | 2015-07-09 |
| K150285 | 2015-03-05 |
| K141980 | 2015-01-26 |
| K142101 | 2014-10-23 |
| K140007 | 2014-04-07 |
| K132719 | 2013-10-04 |
| K131071 | 2013-08-20 |
| K123461 | 2013-04-11 |
Recalls
1 of these is Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.
| Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|
| 2013-05-14 | Class II | Component change control | A component Superior endplate manufactured from a different polymer than specified | 17 units | 2014-02-10 |
PMA Approvals
A premarket approval is the full Class III route, granted on clinical evidence rather than on equivalence to an existing device. It is the highest regulatory bar a device of this type can clear.
| PMA number | Decision | Trade name | Approved to |
|---|---|---|---|
| P000028 | 2004-06-18 | AFFINITY ANTERIOR CERVICAL CAGE SYSTEM | Medtronic Sofamor Danek USA, Inc. |
| P970015 | 2003-09-10 | LT-CAGE PEEK LUMBAR TAPERED FUSION DEVICE | Sofamor Danek |
| P980048 | 2001-04-20 | BAK/CERVICAL (BAK/C) INTERBODY FUSION SYSTEM | Sulzer Spine-Tech |
| P950019 | 1999-03-19 | RAY THREADED FUSION CAGE (TFC) DEVICE WITH INSTRUMENTATION | Stryker Spine |
| P950002 | 1997-06-30 | BAK INTERBODY FUSION SYSTEM | Zimmer Spine, Inc. |
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.