Iop, Inc.
FDA 510(k) & PMA Approved Devices — 9 products
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Total Devices9
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K090078 | KERASYS BIOENGINEERED LAMELLAR PATCH GRAFT | NXM | 2009-05-08 | View |
| 510(k) | K062252 | MOLTENO3 | KYF | 2006-09-27 | View |
| 510(k) | K053622 | SURGISIS OCULAR GRAFT | NXM | 2006-03-15 | View |
| 510(k) | K010852 | OSMED TISSUE EXPANDER | NFM | 2001-08-13 | View |
| 510(k) | K003646 | SUTUREGROOVE WEIGHT SIZING SET | MML | 2001-02-22 | View |
| 510(k) | K994289 | SUTUREGROOVE | MML | 2000-04-17 | View |
| 510(k) | K972143 | MOA BONE / M-SPHERE | HPZ | 1997-10-16 | View |
| 510(k) | K902489 | MODIFIED MOLTENO(TM) IMPLANTS | KYF | 1990-08-14 | View |
| 510(k) | K890598 | MOLTENO IMPLANT | KYF | 1989-02-27 | View |
No matching devices.
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