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 Imm Enterprises with 52 510(k) clearances. The most recent is a 510(k) clearance dated May 9, 1984: KOLLMANN URETHRAL DILATOR.
| May 9, 1984 | KOLLMANN URETHRAL DILATORK841386 · KOE | 510(k) clearances |
| May 9, 1984 | WESTON RECTAL SNAREK841387 · KOA | 510(k) clearances |
| May 9, 1984 | CAT. 7-EAR, NOSE & THROAT DEVICESK840311 · KCP | 510(k) clearances |
| May 1, 1984 | CATEGORY 17-MICROBIOLOGY DEVICESK840304 · HTD | 510(k) clearances |
| Apr 23, 1984 | CAT. 14-CLINICAL TOXIOLOGY DEVICESK840318 · HTD | 510(k) clearances |
| Apr 23, 1984 | CATEGORY 1 CIRCULATORY SYSTEM DEVICEK840305 · DWS | 510(k) clearances |
| Apr 5, 1984 | CAT. 8 DENTAL DEVICESK840312 · EMG | 510(k) clearances |
| Apr 4, 1984 | OP-CON SURG. INSTRUMENT #3K834171 · KOA | 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
