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 14, 2026, FDA's public records list Talley Group with 6 510(k) clearances. The most recent is a 510(k) clearance dated Feb 19, 2016: Venturi Gauze Wound Care Sets with Portal Drain.
| Feb 19, 2016 | Venturi Gauze Wound Care Sets with Portal DrainK151263 · OMP | 510(k) clearances |
| Jan 5, 2016 | VENTURI MiNO TG600/14K143004 · OMP | 510(k) clearances |
| Apr 10, 1992 | TALLEY MICRO SYSTEM/TALLEY RIPPLEBEDK914775 · FNM | 510(k) clearances |
| Feb 11, 1992 | MULTIPULSE SEQUENTIAL COMPRESSION UNITK914774 · IRP | 510(k) clearances |
| Dec 19, 1991 | OXFORD PRESSURE MONITOR/TALLEY PRESSURE MONITORK914776 · JFC | 510(k) clearances |
| Dec 19, 1991 | TALLEY SD.500 SKIN PRESSURE EVALUATORK914780 · IKE | 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
