Home › Device types › POD
Temporary, Internal Use Hemostatic
FDA product code POD · Class 2 · General, Plastic Surgery
29
Registered devices
6
Adverse events
1
Recalls
6
510(k) clearances
Devices with this code
QUIKCLOT — TELEFLEX INCORPORATEDQuikClot — Z-MEDICA, LLCQUIKCLOT — TELEFLEX INCORPORATEDQuikClot — Z-MEDICA, LLCQUIKCLOT — TELEFLEX INCORPORATEDQUIKCLOT — TELEFLEX INCORPORATEDQUIKCLOT — TELEFLEX INCORPORATEDAx-Surgi Surgical Hemostat — Advamedica Inc.QUIKCLOT — TELEFLEX INCORPORATEDQUIKCLOT — TELEFLEX INCORPORATEDQUIKCLOT — TELEFLEX INCORPORATEDQUIKCLOT — TELEFLEX INCORPORATEDQUIKCLOT — TELEFLEX INCORPORATEDQUIKCLOT — TELEFLEX INCORPORATEDQUIKCLOT — TELEFLEX INCORPORATEDQuikClot — Z-MEDICA, LLCQUIKCLOT — TELEFLEX INCORPORATEDQUIKCLOT — TELEFLEX INCORPORATEDQUIKCLOT — TELEFLEX INCORPORATEDAx-Surgi Surgical Hemostat — Advamedica Inc.QUIKCLOT — TELEFLEX INCORPORATEDQuikClot — Z-MEDICA, LLCQUIKCLOT — TELEFLEX INCORPORATEDQUIKCLOT — TELEFLEX INCORPORATED
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2021-10-14 | Beeken Biomedical, LLC | Endotoxin levels exceeded allowable limits. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.