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Data / Medical devices / Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic / United States

FDA-registered makers of Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic in the United States: 25 establishments

25 establishments in the United States are registered with the FDA to make Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic (product code MGQ). 13 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.

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Device
Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic
Product code
MGQ
Country
United States

Makers of Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Amerx Healthcare CorpOldsmar, FL, United StatesRepackager or relabeler, Specification developer2August 12, 1997000api.fda.gov
Deroyal Industries, Inc.Powell, TN, United StatesComplaint file establishment, Specification developer2September 20, 2004000api.fda.gov
MEDLINE INDUSTRIES, LP - NorthfieldNorthfield, IL, United StatesComplaint file establishment, Specification developer2November 8, 2001000api.fda.gov
Aim Medical IncWestwood, MA, United StatesSpecification developer1October 16, 2017000api.fda.gov
Cardinal HealthChicopee, MA, United StatesManufacturer1July 26, 1994000api.fda.gov
Cardinal HealthHazelwood, MO, United StatesSpecification developer1July 26, 1994000api.fda.gov
Cardinal HealthAugusta, GA, United StatesManufacturer1July 26, 1994000api.fda.gov
Ferris MFG. Corp.Fort Worth, TX, United StatesManufacturer1September 22, 1998000api.fda.gov
Human Biosciences, Inc.Martinsburg, WV, United StatesManufacturer1December 2, 2002000api.fda.gov
MPM MedicalMesquite, TX, United StatesSpecification developer1December 18, 1997000api.fda.gov
Nexgel, Inc.Langhorne, PA, United StatesComplaint file establishment, Specification developer1July 23, 2004000api.fda.gov
Stellen Medical, LLCSaint Paul, MN, United StatesManufacturer1October 2, 2000000api.fda.gov
Swiss-American CDMO,LLCCarrollton, TX, United StatesManufacturer1July 18, 1994000api.fda.gov
3-D Matrix, Inc.Newton, MA, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Biomed Laboratories LLCDallas, TX, United StatesContract manufacturer0000api.fda.gov
CG Converting And Packaging, LLCGranbury, TX, United StatesContract manufacturer0000api.fda.gov
Deroyal Industries, Inc.Maynardville, TN, United StatesContract manufacturer0000api.fda.gov
Deroyal Industries, Inc.New Tazewell, TN, United StatesContract manufacturer0000api.fda.gov
Forward Science Technologies LLCHouston, TX, United StatesManufacturer0000api.fda.gov
Inter-Med, Inc.Racine, WI, United StatesManufacturer0000api.fda.gov
Lindo ManufacturingSwansea, MA, United StatesContract manufacturer0000api.fda.gov
Medline Industries, LPNorth Mankato, MN, United StatesContract manufacturer0000api.fda.gov
Primus Pharmaceuticals, Inc.Scottsdale, AZ, United StatesSpecification developer0000api.fda.gov
SPAN PACKAGING SERVICES d.b.a. MULTI-PACK SOLUTIONSGreenville, SC, United StatesContract manufacturer, Manufacturer for export0000api.fda.gov
Sterigenics US LLCFort Worth, TX, United StatesContract sterilizer, Manufacturer for export0000api.fda.gov

Updated November 3, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.