Osteogenics Biomedical, Inc.
FDA 510(k) & PMA Approved Devices — 8 products
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Total Devices8
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K201187 | Cytoplast Titanium-Reinforced PTFE Membranes | NPK | 2021-01-23 | View |
| 510(k) | K171774 | RPM Reinforced PTFE Mesh | NPK | 2017-10-19 | View |
| 510(k) | K093719 | PRO-FIX PRECISION FIXATION SYSTEM MODEL PFM#, PFB#, PFT# | DZL | 2010-03-01 | View |
| 510(k) | K072076 | CYTOPLAST PTFE SUTURE | NBY | 2007-10-31 | View |
| 510(k) | K013764 | IMMIX BONE GRAFT EXTENDER | KKY | 2002-05-16 | View |
| 510(k) | K003028 | CYTOPLAST SUTURE; CS-0318, CS-0416, CS-0418, CS-0513, CS-0513PC, CS-0516HC | NBY | 2000-11-24 | View |
| 510(k) | K993610 | CYTOPLAST RESORB, MODELS R-250, RP-250, RU-250, RPS-250, RPL-250 | LYC | 2000-03-02 | View |
| 510(k) | K984230 | OSTEO-MESH TM-300 | JEY | 1999-02-04 | View |
No matching devices.
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