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 IBL GmbH with 6 510(k) clearances. The most recent is a 510(k) clearance dated Oct 3, 2005: TRICAT RIA (ADRENALIN/NORADRENALIN/DOPAMINE); KATCOMBI RIA (ADRENALIN/NORADRENALIN); NOR….
| Date | Record | Source |
|---|---|---|
| Oct 3, 2005 | TRICAT RIA (ADRENALIN/NORADRENALIN/DOPAMINE); KATCOMBI RIA (ADRENALIN/NORADRENALIN); NORADRENALIN RIAK051969 · CHQ | 510(k) clearances |
| Sep 24, 2004 | LUMINESCENT IMMUNOASSAY KIT FOR THE DETECTION OF ESTRADIOL IN SALIVA AND SERUMK041349 · CHP | 510(k) clearances |
| Jul 22, 2004 | LUMINESCENT IMMUNOASSAY KIT FOR THE DETECTION OF PROGESTERONE IN SALIVAK040923 · JLS | 510(k) clearances |
| Feb 27, 2004 | LUMINESCENT IMMUNOASSAY KIT FOR THE DETECTION OF TESTOSTERONE IN SERUM AND SALIVAK033786 · JIT | 510(k) clearances |
| Jan 13, 2004 | IBL C3D-CIC EIA TESTK032796 · CZW | 510(k) clearances |
| Aug 29, 2003 | IBL C1Q-CIC CIA TESTK032254 · DAK | 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