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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 2 of 9
DeviceModel / ReferenceRegistriesClassStatus
ComfortFoam Border 43680
FDA UDI
Class IActive
DermaBlue+Foam Transfer Healogics by DermaRite 94131
FDA UDI
UActive
DermaBlue + Foam 76040514
FDA UDI
UActive
ComfortFoam Border 00318E
FDA UDI
Class IActive
Dermaginate/Ag Healogics by DermaRite 93514
FDA UDI
UActive
StingFree Wand 11239
FDA UDI
Class IActive
Sterile Bordered Gauze Healogics by DermaRite 93139
FDA UDI
Class IActive
ComfortFoam 44680
FDA UDI
Class IActive
DermaFilm HD 33660
FDA UDI
Class IActive
ComfortFoam Healogics by DermaRite 93191
FDA UDI
Class IActive
SafeWash Saline 00245
FDA UDI
Class IIActive
Adhesive Tape Remover Pads 82100
FDA UDI
Class IActive
ComfortFoam 44330
FDA UDI
Class IActive
ComfortFoam Border Lite Healogics by DermaRite 93253
FDA UDI
Class IActive
Sterile Bordered Gauze Healogics by DermaRite 93131
FDA UDI
Class IActive
DermaBlue + Foam Healogics by DermaRite 94111
FDA UDI
UActive
DermaSyn 00248
FDA UDI
Class IActive
UnnaRite w/ Zinc Healogics by DermaRite 93972
FDA UDI
Class IActive
Sterile Bordered Gauze 11414
FDA UDI
Class IActive
DermaFoam 00291E
FDA UDI
Class IActive
DermaBlue + Foam 75081614
FDA UDI
UUnknown
DermaLevin Healogics by DermaRite 93552
FDA UDI
Class IActive
DermaFilm Heel/Elbow 00299E
FDA UDI
Class IActive
DermaView II 93655
FDA UDI
Class IActive
ComfortFoam Border Sacral 43880
FDA UDI
Class IActive
DermaGinate/Ag 00535E
FDA UDI
UActive
DermaFilm X-Thin Clear with Grid 31240
FDA UDI
Class IActive
ComfortFoam Border Healogics by Dermarite 93219
FDA UDI
Class IActive
ComfortFoam/Ag Border Healogics by DermaRite 93292
FDA UDI
UActive
Bordered Gauze 00255
FDA UDI
Class IActive
DermaCol Healogics by Dermarite 93312
FDA UDI
UActive
DermaGinate 00272E
FDA UDI
Class IActive
Sterile Bordered Gauze 11410
FDA UDI
Class IActive
DermaView II 00252E
FDA UDI
Class IActive
DermaCol Ag 00502E
FDA UDI
UActive
StayStrips 72183
FDA UDI
Class IActive
DermaSyn/Ag 00510
FDA UDI
UActive
DermaGinate 00274E
FDA UDI
Class IActive
ComfortFoam Border Heel 43580
FDA UDI
Class IActive
DermaBlue+Foam Healogics by DermaRite 94113
FDA UDI
UActive
DermaFoam 00291E
FDA UDI
Class IActive
Xeroform Gauze Dressing 24440
FDA UDI
Class IActive
DermaFilm X-Thin Clear with Grid 00219E
FDA UDI
Class IActive
DermaView II Island Dressing 16310
FDA UDI
Class IActive
DermaBlue + Foam Transfer 76040418
FDA UDI
UActive
AquaRite Extra CMC 40450
FDA UDI
Class IActive
Sting Free Wand 11238
FDA UDI
Class IActive
StayStrips 72540
FDA UDI
Class IActive
DermaSyn 11245
FDA UDI
Class IActive
DermaFoam 00290E
FDA UDI
Class IActive

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