FirmLabelled 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 Inman Liebelt Corp. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Aug 9, 1991: INTRAVASCULAR CATHETER SECURMENT DEVICE.
| Aug 9, 1991 | INTRAVASCULAR CATHETER SECURMENT DEVICEK912211 · KMK | 510(k) clearances |
| Jul 26, 1991 | URETERAL CATHETER HOLDERK912146 · KNY | 510(k) clearances |
| May 10, 1991 | UCEZ - STERILE LENS FOG REDUCTION DEVICEK905590 · OCT | 510(k) clearances |
| Apr 12, 1991 | ILC FORCEPS PADSK905583 · HDA | 510(k) clearances |
| Oct 26, 1990 | ILC LEG BAG HOLDERK903611 · FAQ | 510(k) clearances |
| Oct 19, 1990 | O.R. TIP CLEANERK903610 · GEI | 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
