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 15, 2026, FDA's public records list Acacia Laboratories, Inc. with 12 510(k) clearances. The most recent is a 510(k) clearance dated Jul 26, 1995: STERIGAUZE GEL DRESSING.
| Jul 26, 1995 | STERIGAUZE GEL DRESSINGK952419 · MGQ | 510(k) clearances |
| Jul 12, 1995 | STERIGAUZE WET DRESSINGK952420 · KMF | 510(k) clearances |
| Jul 11, 1995 | STERICARE WOUND CARE GELK951861 · MGQ | 510(k) clearances |
| Jun 23, 1995 | PREFILLED SYRINGE FOR INFLATION OF FOLEY CATHETERK952414 · KNY | 510(k) clearances |
| May 15, 1995 | HYDRACARE ABSORBENT WOUND DRESSINGK951914 · KMF | 510(k) clearances |
| Mar 24, 1995 | HORIZON FOLEY CATHETERIZATION TRAY WITHOUT CATHETERK950344 · FCM | 510(k) clearances |
| Mar 12, 1992 | STERILE PLASTIC DRAPEK913408 · KKX | 510(k) clearances |
| May 7, 1990 | STERILE SUCTION TUBING SETK901761 · BYY | 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
