Data / Medical devices / Intervertebral Fusion Device With Bone Graft, Lumbar / Taiwan
FDA-registered makers of Intervertebral Fusion Device With Bone Graft, Lumbar in Taiwan: 5 establishments
5 establishments in Taiwan are registered with the FDA to make Intervertebral Fusion Device With Bone Graft, Lumbar (product code MAX). 3 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Intervertebral Fusion Device With Bone Graft, Lumbar
- Product code
- MAX
- Country
- Taiwan
Makers of Intervertebral Fusion Device With Bone Graft, Lumbar in Taiwan
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Paonan Biotech Co., Ltd | Taipei, Taiwan | Manufacturer | 2 | January 25, 2019 | 0 | 0 | 0 | api.fda.gov |
| Baui Biotech Co., Ltd. | New Taipei City, Taiwan | Manufacturer | 1 | April 14, 2020 | 0 | 0 | 0 | api.fda.gov |
| BioGend Therapeutics Co., Ltd | Taipei City, Taiwan | Specification developer | 1 | March 6, 2024 | 0 | 0 | 0 | api.fda.gov |
| Intai Technology Corp. Implants Business Unit | Taichung City, Taiwan | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Miing Wei Co., Ltd. | Tsao-Twon Nantou, Taiwan | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.