Company ยท US
Iop, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1989 to 2009. Name variants (Inc, Corp, punctuation) are merged.
9510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| May 8, 2009 | K090078 | KERASYS BIOENGINEERED LAMELLAR PATCH GRAFT Iop, Inc. | NXM |
| Sep 27, 2006 | K062252 | MOLTENO3 Iop, Inc. | KYF |
| Mar 15, 2006 | K053622 | SURGISIS OCULAR GRAFT Iop, Inc. | NXM |
| Aug 13, 2001 | K010852 | OSMED TISSUE EXPANDER Iop, Inc. | NFM |
| Feb 22, 2001 | K003646 | SUTUREGROOVE WEIGHT SIZING SET Iop, Inc. | MML |
| Apr 17, 2000 | K994289 | SUTUREGROOVE Iop, Inc. | MML |
| Oct 16, 1997 | K972143 | MOA BONE / M-SPHERE Iop, Inc. | HPZ |
| Aug 14, 1990 | K902489 | MODIFIED MOLTENO(TM) IMPLANTS Iop, Inc. | KYF |
| Feb 27, 1989 | K890598 | MOLTENO IMPLANT Iop, Inc. | KYF |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||