Home › Device types › MGP
Dressing, Wound And Burn, Occlusive
FDA product code MGP · Class U · Unknown
46
Registered devices
102
Adverse events
1
Recalls
80
510(k) clearances
Devices with this code
DERMAGRAN®-B — Derma Sciences Canada IncRUSCH — TELEFLEX INCORPORATEDSTRADIS — STRADIS MEDICAL, LLCRUSCH — TELEFLEX INCORPORATEDSilon-TSR Face Mask Kit — Bio Med Sciences, Inc.PFAB SMALL — SUN SCIENTIFIC, INC.Silon-TSR 11x12 — Bio Med Sciences, Inc.Silon-TSR 5x5 — Bio Med Sciences, Inc.CVS Health™ — WOONSOCKET PRESCRIPTION CENTER, INCORPORATEDSTRADIS — STRADIS MEDICAL, LLCRUSCH — TELEFLEX INCORPORATEDSTRADIS — STRADIS MEDICAL, LLCPFAB Large — SUN SCIENTIFIC, INC.ACTICOAT 4" X 8" — SMITH & NEPHEW MEDICAL LIMITEDSilon-TSR Face Mask Design — Bio Med Sciences, Inc.STRADIS — STRADIS MEDICAL, LLCACTICOAT 3 5" X 5" — SMITH & NEPHEW MEDICAL LIMITEDSTRADIS — STRADIS MEDICAL, LLCACTICOAT 2"X2" — SMITH & NEPHEW MEDICAL LIMITEDRUSCH — TELEFLEX INCORPORATEDDERMAGRAN®-B — Derma Sciences Canada IncNEODERM — Conmed CorporationSTRADIS — STRADIS MEDICAL, LLCDERMAGRAN®-B — Derma Sciences Canada Inc
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2011-02-11 | Hartmann USA, Inc | Misbranded; the expiry date on the primary packing incorrectly indicates 2010-10, instead of 2015-10. Consignees were notified by letter on/about 02/11/2011. Th |
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.