510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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MGPUnclassified

Dressing, Wound And Burn, Occlusive

Unknown
FDA source (opens on fda.gov)

MGP is the FDA product code for Dressing, Wound And Burn, Occlusive. As of , FDA records hold 80 510(k) clearances under this code, the most recent dated , and one recall.

Classification record

Product code
MGP
Device name
Dressing, Wound And Burn, Occlusive
Device class
Unclassified
Review panel
Unknown
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
80
Ingested recalls
1

Clearances, product code MGP

By decision year
80 clearances under product code MGP with a decision year between 1991 and 2001, 1995 the highest year at 19.
Show the numbers
510(k) clearances under FDA product code MGP by decision year
YearClearances
19914
19925
19935
19947
199519
19969
19979
199812
19997
20013

Applicants with the most clearances

Product code MGP
Applicants holding the most 510(k) clearances under product code MGP
ApplicantClearances
Polymedica Industries, Inc.6
Acutek Adhesive Specialties, Inc.4
Bioderm, Inc.3
Dermaphylyx, Inc.3
Euromed, Inc.3
Innovative Technologies, Ltd.3
Beiersdorf, Inc.2
Bio Med Sciences, Inc.2
Biocore Medical Technologies, Inc.2
Calgon Vestal Div.2

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 21 companies shown, in name order