TxTiHA®
Ti 6Al 4V (ELI); Hydroxyapatite
14manufacturers in China registered for this device type
52catalogue numbers in this listing
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 | Inno-Health Technology Co., Ltd., Taiwan |
|---|---|
| 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, Contract steriliser, Manufacturer |
| 510(k) | K201614 |
| Record published | 2021-09-30 |
| Record revised | 2026-02-10 (version 4) |
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 |
| Packaging | Carton |
| Sizes | Width 10 to 12 mm; height 7 to 16 mm; length 28 to 33 mm; angle 5 to 12.5 ° |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| TXT10122805 | Width 10 mm | In distribution |
| TXT12153310 | Width 12 mm | In distribution |
| TXT12113305 | Width 12 mm | In distribution |
| TXT12163312 | Width 12 mm | In distribution |
| TXT12143312 | Width 12 mm | In distribution |
| TXT10092812 | Width 10 mm | In distribution |
| TXT10142812 | Width 10 mm | In distribution |
| TXT10112805 | Width 10 mm | In distribution |
| TXT10092810 | Width 10 mm | In distribution |
| TXT10132812 | Width 10 mm | In distribution |
| TXT12143310 | Width 12 mm | In distribution |
| TXT12163310 | Width 12 mm | In distribution |
| TXT12103312 | Width 12 mm | In distribution |
| TXT10142805 | Width 10 mm | In distribution |
| TXT12113310 | Width 12 mm | In distribution |
| TXT10112812 | Width 10 mm | In distribution |
| TXT12143305 | Width 12 mm | In distribution |
| TXT10142810 | Width 10 mm | In distribution |
| TXT10132805 | Width 10 mm | In distribution |
| TXT12123305 | Width 12 mm | In distribution |
| TXT12123312 | Width 12 mm | In distribution |
| TXT10152810 | Width 10 mm | In distribution |
| TXT10162805 | Width 10 mm | In distribution |
| TXT12153312 | Width 12 mm | In distribution |
| TXT10072805 | Width 10 mm | In distribution |
| TXT12093305 | Width 12 mm | In distribution |
| TXT12153305 | Width 12 mm | In distribution |
| TXT12093310 | Width 12 mm | In distribution |
| TXT10162810 | Width 10 mm | In distribution |
| TXT10132810 | Width 10 mm | In distribution |
| TXT10092805 | Width 10 mm | In distribution |
| TXT10082805 | Width 10 mm | In distribution |
| TXT10122812 | Width 10 mm | In distribution |
| TXT12133312 | Width 12 mm | In distribution |
| TXT12163305 | Width 12 mm | In distribution |
| TXT10162812 | Width 10 mm | In distribution |
| TXT12133305 | Width 12 mm | In distribution |
| TXT10152812 | Width 10 mm | In distribution |
| TXT10152805 | Width 10 mm | In distribution |
| TXT10082810 | Width 10 mm | In distribution |
| TXT12113312 | Width 12 mm | In distribution |
| TXT12133310 | Width 12 mm | In distribution |
| TXT10102810 | Width 10 mm | In distribution |
| TXT12103310 | Width 12 mm | In distribution |
| TXT10112810 | Width 10 mm | In distribution |
| TXT12103305 | Width 12 mm | In distribution |
| TXT10102812 | Width 10 mm | In distribution |
| TXT12083305 | Width 12 mm | In distribution |
| TXT10122810 | Width 10 mm | In distribution |
| TXT10102805 | Width 10 mm | In distribution |
| TXT12123310 | Width 12 mm | In distribution |
| TXT12093312 | Width 12 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
Recalls Naming This Product
1 recall names this product by its own identifier, the 510(k) it is cleared under.
| Recalled by | Identified by | Initiated | FDA class | Root cause | Reason | Quantity |
|---|---|---|---|---|---|---|
| Innovasis, Inc. | 510(k) number | 2024-08-14 | Class II | Device Design | Due to interfacing issues between the implant trial and inserter of the lumbar intervertebral fusion device. | 568 devices |
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.