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 Medikmark, Inc. with 8 510(k) clearances. The most recent is a 510(k) clearance dated Oct 2, 1995: IV START KIT.
| Date | Record | Source |
|---|---|---|
| Oct 2, 1995 | IV START KITK953474 · FPA | 510(k) clearances |
| Oct 7, 1994 | UPPER EXTERMITY DRAPE KITK923960 · KKX | 510(k) clearances |
| Jun 15, 1994 | MINOR LAP SETK921732 · KOH | 510(k) clearances |
| Jun 15, 1994 | C-SECTION PACKK921730 · KOH | 510(k) clearances |
| Jun 15, 1994 | TRACHEOSTOMY CARE TRAYK921733 · JOH | 510(k) clearances |
| Apr 23, 1992 | LACERATION TRAYSK920341 · KKX | 510(k) clearances |
| Apr 23, 1992 | SUTURE REMOVAL KITK920340 · KKX | 510(k) clearances |
| Apr 23, 1992 | DRESSING CHANGE TRAYK920339 · FRG | 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
