Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Iop, Inc. with 9 510(k) clearances. The most recent is a 510(k) clearance dated May 8, 2009: KERASYS BIOENGINEERED LAMELLAR PATCH GRAFT.
| Date | Record | Source |
|---|---|---|
| May 8, 2009 | KERASYS BIOENGINEERED LAMELLAR PATCH GRAFTK090078 · NXM | 510(k) clearances |
| Sep 27, 2006 | MOLTENO3K062252 · KYF | 510(k) clearances |
| Mar 15, 2006 | SURGISIS OCULAR GRAFTK053622 · NXM | 510(k) clearances |
| Aug 13, 2001 | OSMED TISSUE EXPANDERK010852 · NFM | 510(k) clearances |
| Feb 22, 2001 | SUTUREGROOVE WEIGHT SIZING SETK003646 · MML | 510(k) clearances |
| Apr 17, 2000 | SUTUREGROOVEK994289 · MML | 510(k) clearances |
| Oct 16, 1997 | MOA BONE / M-SPHEREK972143 · HPZ | 510(k) clearances |
| Aug 14, 1990 | MODIFIED MOLTENO(TM) IMPLANTSK902489 · KYF | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
