Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled 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 15, 2026, FDA's public records list Innerdyne Medical, Inc. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Oct 11, 1994: INNERDYNE STEP TROCAR EXPANDABLE PORT, S.T.E.P..
| Oct 11, 1994 | INNERDYNE STEP TROCAR EXPANDABLE PORT, S.T.E.P.K943253 · GCJ | 510(k) clearances |
| Sep 27, 1994 | SINGLE STICK RADIALLY EXPANDING DILATORK943056 · GCJ | 510(k) clearances |
| Apr 25, 1994 | INNERDYNE SINGLE-STICK RADIALLY EXPANDING DILATORK940428 · GCJ | 510(k) clearances |
| Apr 18, 1994 | INNERDYNE STEP TROCAR EXPANDABLE PORT, S.T.E.P.K940232 · GCJ | 510(k) clearances |
| Dec 27, 1993 | INNERDYNE MEDICAL LAPAROSCOPIC SPHINCTEROTOMY KITK932692 · GCJ | 510(k) clearances |
| Oct 15, 1993 | INTHERM RADIALLY EXPANDING DILATING INTRODUCERK931489 · DYB | 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
