Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Gibson Laboratories with 4 510(k) clearances and 1 device recall. The most recent is a device recall dated Jan 20, 2017: Blastomyces dermatitidis Antiserum 1 mL vial GIBSON BIOSCIENCE. Catalog 200265 Inten….
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Jan 20, 2017 | Blastomyces dermatitidis Antiserum 1 mL vial GIBSON BIOSCIENCE. Catalog 200265 Intended for identification of the systemic fungal pathogClass II · The firm information that the product was reporting false positive results | Device recalls |
| Feb 29, 1996 | GIBSON ID-M. CAT.K955826 · JTO | 510(k) clearances |
| Nov 20, 1995 | GIBSON ID A.E. TESTK953247 · JTO | 510(k) clearances |
| Dec 17, 1990 | SAF FIXATIVEK905120 · LIO | 510(k) clearances |
| Dec 4, 1990 | P AND T MEDIUMK904773 · JTW | 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
