Home › Device types › MGP
Dressing, Wound And Burn, Occlusive
FDA product code MGP · Class U · Unknown
46
Registered devices
95
Adverse events
1
Recalls
80
510(k) clearances
Devices with this code
Dual-Dress 50 11x12 — Bio Med Sciences, Inc.PFAB SMALL — SUN SCIENTIFIC, INC.Silon-TSR 5x5 — Bio Med Sciences, Inc.STRADIS — STRADIS MEDICAL, LLCSTRADIS — STRADIS MEDICAL, LLCACTICOAT 3 5" X 5" — SMITH & NEPHEW MEDICAL LIMITEDPFAB Medium Crescent — SUN SCIENTIFIC, INC.DERMAGRAN®-B — Derma Sciences Canada IncSTRADIS — STRADIS MEDICAL, LLCDERMAGRAN®-B — Derma Sciences Canada IncSTRADIS — STRADIS MEDICAL, LLCSTRADIS HEALTHCARE — STRADIS MEDICAL, LLCSTRADIS — STRADIS MEDICAL, LLCRUSCH — TELEFLEX INCORPORATEDSTRADIS — STRADIS MEDICAL, LLCACTICOAT 4"X48" — SMITH & NEPHEW MEDICAL LIMITEDSTRADIS — STRADIS MEDICAL, LLCACTICOAT 2"X2" — SMITH & NEPHEW MEDICAL LIMITEDSTRADIS — STRADIS MEDICAL, LLCSilon-TSR 5x10 — Bio Med Sciences, Inc.RUSCH — TELEFLEX INCORPORATEDRUSCH — TELEFLEX INCORPORATEDACTICOAT 4" X 4" — SMITH & NEPHEW MEDICAL LIMITEDACTICOAT 8"X16" — SMITH & NEPHEW MEDICAL LIMITED
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 |
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