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 Faulding Medical Device with 6 510(k) clearances. The most recent is a 510(k) clearance dated Jul 18, 1997: STERILE AMBULATORY RESERVOIR 60ML/100ML.
| Jul 18, 1997 | STERILE AMBULATORY RESERVOIR 60ML/100MLK962159 · MRZ | 510(k) clearances |
| May 6, 1997 | SAFE-CONNECT I.V. SETK970909 · FPA | 510(k) clearances |
| May 1, 1997 | SAFE-CONNECT VIAL DISPENSING SPIKEK970789 · LHI | 510(k) clearances |
| May 1, 1997 | SAFE-CONNECT Y-SITE ADAPTER CATALOG NO. 681518K971266 · FPA | 510(k) clearances |
| Apr 22, 1997 | SAFE-CONNECT I.V. EXTENSION SETK970524 · FPA | 510(k) clearances |
| Nov 15, 1996 | SAFECONNECT VALVE (CATALOG NO. XXXX)K955775 · FPA | 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
