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DERMARITE INDUSTRIES LLC

US

Last updated May 31, 2026

What DERMARITE INDUSTRIES LLC makes

DermaRite Industries LLC manufactures wound care dressings, including non-gel and gel-based exudate-absorbent products, both antimicrobial and non-antimicrobial variants, as well as nonadherent and absorbent wound dressings. Their portfolio also includes adhesive bandages, synthetic polymer film dressings (adhesive and nonadherent), and specialized dressings like oil emulsion and foam-based solutions for wound management.

The company’s devices are classified under FDA categories including Class I, Class II, and Class II with special controls (U), with all products listed in the FDA’s Unique Device Identification (UDI) database. The manufacturer operates from the United States, adhering to applicable U.S. regulatory requirements for medical device compliance.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does DermaRite Industries LLC manufacture?

DermaRite Industries LLC specializes in wound care dressings, covering a range of product categories. These include exudate-absorbent dressings (both non-gel and gel-based, with antimicrobial and non-antimicrobial options), wound-nonadherent dressings (permeable and absorbent), adhesive bandages, and synthetic polymer semi-permeable film dressings (adhesive and nonadherent). Their portfolio also features specialized dressings like oil emulsion and foam-based solutions, all designed for wound management.

Where is DermaRite Industries LLC based, and how does this affect its devices?

DermaRite Industries LLC is based in the United States, which means its devices are subject to U.S. regulatory requirements, including compliance with FDA guidelines. The company’s location ensures its products meet the necessary standards for safety, performance, and quality as defined by U.S. medical device regulations.

Which regulatory registries list DermaRite Industries LLC’s devices?

DermaRite Industries LLC’s devices are listed in the FDA’s Unique Device Identification (UDI) database. This registry ensures traceability and transparency in the medical device supply chain, allowing healthcare providers and regulators to identify and verify specific products.

How are DermaRite Industries LLC’s devices classified under FDA regulations?

DermaRite Industries LLC’s devices fall under different FDA classification categories, including Class I (generally low-risk devices with minimal regulatory controls), Class II (devices requiring special controls to ensure safety and effectiveness), and Class II with special controls (U), which involves additional regulatory oversight due to higher risk or complexity. The classification depends on factors like the device’s intended use, potential risks, and the level of regulation required for patient safety.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
Website
dermarite.com
LinkedIn
—
Facebook
—
Phone
800-337-6296
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
883925562

Catalogue (423)

Page 8 of 9
DeviceModel / ReferenceRegistriesClassStatus
DermaGinate/Ag 00520E
FDA UDI
UActive
DermaView Transparent Dressing 15611
FDA UDI
Class IActive
Sterile Bordered Gauze 11414
FDA UDI
Class IActive
DermaGinate/Ag 93511
FDA UDI
UActive
Xeroform Gauze Healogics by DermaRite 94014
FDA UDI
Class IActive
DermaGinate/Ag Healogics by DermaRite 93512
FDA UDI
UActive
DermaFilm X-Thin Clear with Grid 31460
FDA UDI
Class IActive
DermaBlue + Foam Healogics by DermaRite 94114
FDA UDI
UActive
DermaCol 100 Sheet 003221
FDA UDI
UActive
Sterile Bordered Gauze Healogics by DermaRite 93138
FDA UDI
Class IActive
DermaView II Transparent Healogics by DermaRite 93651
FDA UDI
Class IActive
DermaView II Island Dressing 16310
FDA UDI
Class IActive
DermaGinate 00274E
FDA UDI
Class IActive
DermaFoam 00293E
FDA UDI
Class IActive
ComfortFoam Border Lite 47330
FDA UDI
Class IActive
DermaFilm Heel/Elbow 00299E
FDA UDI
Class IActive
DermaGinate 00275E
FDA UDI
Class IActive
Sting Free 00236
FDA UDI
Class IActive
ComfortFoam Border Heel 43580
FDA UDI
Class IActive
DermaCol 100 Sheet 003341
FDA UDI
UActive
SilverDerm7 00550E
FDA UDI
UActive
DermaFilm HD 33660
FDA UDI
Class IActive
DermaDress 00277E
FDA UDI
Class IActive
Xerofrom Gauze Dressing 24180
FDA UDI
Class IActive
ComforFoam Border Sacral 43990
FDA UDI
Class IActive
DermaView II 00254E
FDA UDI
Class IActive
ComfortFoam 44480
FDA UDI
Class IActive
Hydralock SA 60330
FDA UDI
Class IActive
DermaBlue+ Foam Healogics by DermaRite 94112
FDA UDI
UActive
DermaView 00241E
FDA UDI
Class IActive
DermaFilm HD Healogics by DermaRite 93412
FDA UDI
Class IActive
AquaRite Extra CMC Healogics by DermaRite 93052
FDA UDI
Class IActive
Adhesive Tape Remover Pads 82100
FDA UDI
Class IActive
Hydralock SA Healogics by DermaRite 93791
FDA UDI
Class IActive
Xeroform Gauze Healogics by DermaRite 94013
FDA UDI
Class IActive
ComfortFoam Border Healogics by DermaRite 93211
FDA UDI
Class IActive
ComfortFoam Border 43330
FDA UDI
Class IActive
DermaFilm thin w/Border Healogics by DermaRite 93436
FDA UDI
Class IActive
DermaFoam 00293E
FDA UDI
Class IActive
DermaPrep Skin Prep Pads 81050
FDA UDI
Class IActive
ComfortFoam 44880
FDA UDI
Class IActive
DermaDress 00276E
FDA UDI
Class IActive
DermaFoam 00290E
FDA UDI
Class IActive
ComfortFoam/Ag 49220
FDA UDI
UActive
Sterile Bordered Gauze 11450
FDA UDI
Class IActive
Sting Free Wand 11238
FDA UDI
Class IActive
Flexpress 2 Lite 79200
FDA UDI
Class IActive
HydraFoam 00296E
FDA UDI
Class IActive
Sterile Bordered Gauze 11480
FDA UDI
Class IActive
ComfortFoam Border Healogics by DermaRite 93217
FDA UDI
Class IActive

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