Inter-Med, 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) | K253337 | REGEN Bioactive Cement | EMA | 2026-04-15 | View |
| 510(k) | K241489 | ReminGel | LBH | 2025-01-08 | View |
| 510(k) | K241457 | Vista BC Putty | KIF | 2024-08-28 | View |
| 510(k) | K241354 | Sealer Solvent | KJJ | 2024-08-27 | View |
| 510(k) | K221811 | Vista BC Sealer | KIF | 2022-11-21 | View |
| 510(k) | K211721 | PS System | NYL | 2021-12-02 | View |
| 510(k) | K112250 | CHX=CHX PLUS | KJJ | 2011-10-28 | View |
| 510(k) | K082470 | SODIUM HYPOCHLORITE 3 & 6% SOLUTION AND 6% WITH WETTING AGENTS TO LOWER SURFACE TENSION MARKETED AS CHLOR-XTRA | KJJ | 2009-04-03 | View |
No matching devices.
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