Tspace® Peek
Tspace Peek Implant 5° 30X11.5X10MM
14manufacturers in China registered for this device type
69catalogue numbers in this listing
1recall
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 | Aesculap AG, Germany |
|---|---|
| FDA product code | MAX |
| Device type | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Device class | Class 2 |
| Regulation | 21 CFR 888.3080 |
| Establishment | Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter |
| Record published | 2015-11-11 |
| Record revised | 2025-11-13 (version 6) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Label carries | lot or batch number, expiry date |
| Distribution end date | 2025-10-28 |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| SN340P | Degree (°) : 5.000 DEG | Withdrawn |
| SN317P | Degree (°) : 5.000 DEG | Withdrawn |
| SN367P | Length : 34.000 MM | Withdrawn |
| FJ319P | Length : 30.000 MM | Withdrawn |
| SJ970P | Length : 34.000 MM | Withdrawn |
| FJ321P | Length : 30.000 MM | Withdrawn |
| SJ943P | Length : 30.000 MM | Withdrawn |
| SJ912P | Length : 26.000 MM | Withdrawn |
| SN339P | Degree (°) : 5.000 DEG | Withdrawn |
| SN307P | Degree (°) : 5.000 DEG | Withdrawn |
| FJ687P | Length : 26.000 MM | Withdrawn |
| SN370P | Height : 10.000 MM | Withdrawn |
| SN343P | Height : 13.000 MM | Withdrawn |
| SJ917P | Length : 26.000 MM | Withdrawn |
| SJ910P | Length : 26.000 MM | Withdrawn |
| FJ693P | Length : 26.000 MM | Withdrawn |
| SN373P | Length : 34.000 MM | Withdrawn |
| SJ937P | Length : 30.000 MM | Withdrawn |
| SN311P | Length : 26.000 MM | Withdrawn |
| SN314P | Length : 26.000 MM | Withdrawn |
| SJ973P | Length : 34.000 MM | Withdrawn |
| SJ907P | Height : 7.000 MM | Withdrawn |
| SJ969P | Length : 34.000 MM | Withdrawn |
| SJ938P | Length : 30.000 MM | Withdrawn |
| SN337P | Length : 30.000 MM | Withdrawn |
| SN312P | Height : 12.000 MM | Withdrawn |
| SN368P | Degree (°) : 5.000 DEG | Withdrawn |
| SN369P | Degree (°) : 5.000 DEG | Withdrawn |
| SN308P | Length : 26.000 MM | Withdrawn |
| FJ325P | Length : 30.000 MM | Withdrawn |
| SJ911P | Length : 26.000 MM | Withdrawn |
| SN371P | Height : 11.000 MM | Withdrawn |
| SJ939P | Length : 30.000 MM | Withdrawn |
| FJ695P | Degree (°) : 5.000 DEG | Withdrawn |
| SN309P | Degree (°) : 5.000 DEG | Withdrawn |
| FJ691P | Length : 26.000 MM | Withdrawn |
| SN315P | Length : 26.000 MM | Withdrawn |
| FJ317P | Length : 30.000 MM | Withdrawn |
| SN372P | Height : 12.000 MM | Withdrawn |
| SJ908P | Length : 26.000 MM | Withdrawn |
| FJ323P | Length : 30.000 MM | Withdrawn |
| SN344P | Degree (°) : 5.000 DEG | Withdrawn |
| SN374P | Length : 34.000 MM | Withdrawn |
| SJ915P | Length : 26.000 MM | Withdrawn |
| FJ697P | Length : 26.000 MM | Withdrawn |
| SJ977P | Length : 34.000 MM | Withdrawn |
| SJ909P | Length : 26.000 MM | Withdrawn |
| SJ945P | Length : 30.000 MM | Withdrawn |
| SN347P | Height : 17.000 MM | Withdrawn |
| FJ689P | Height : 9.000 MM | Withdrawn |
| SJ971P | Length : 34.000 MM | Withdrawn |
| SJ940P | Length : 30.000 MM | Withdrawn |
| SJ968P | Length : 34.000 MM | Withdrawn |
| SJ942P | Length : 30.000 MM | Withdrawn |
| SN342P | Degree (°) : 5.000 DEG | Withdrawn |
| SN345P | Length : 30.000 MM | Withdrawn |
| SJ972P | Length : 34.000 MM | Withdrawn |
| SJ947P | Length : 30.000 MM | Withdrawn |
| SJ975P | Length : 34.000 MM | Withdrawn |
| FJ327P | Length : 30.000 MM | Withdrawn |
| SN375P | Length : 34.000 MM | Withdrawn |
| SJ913P | Length : 26.000 MM | Withdrawn |
| SN313P | Height : 13.000 MM | Withdrawn |
| SN341P | Height : 11.000 MM | Withdrawn |
| SN338P | Length : 30.000 MM | Withdrawn |
| SJ967P | Length : 34.000 MM | Withdrawn |
| SJ941P | Length : 30.000 MM | Withdrawn |
| SN310P | Height : 10.000 MM | Withdrawn |
| SN377P | Degree (°) : 5.000 DEG | Withdrawn |
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
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 |
|---|---|---|---|---|---|
| 2013-06-18 | Class II | Employee error | Aesculap Implant Systems, LLC initiated a recall of the Aesculap Prospace PEEK 5 degree Implant – 8 x 8.5 x 22 mm (SN038P) because the device is incorrectly etched with an 8 degree lordosis instead of a 5 degree lordosis. The device is labe | 9 | 2014-01-13 |
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.