Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

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 5 of 9
DeviceModel / ReferenceRegistriesClassStatus
Xeroform Gauze Dressing 24220
FDA UDI
Class IActive
DermaSyn 00247
FDA UDI
Class IActive
AquaDerm 00322E
FDA UDI
Class IActive
ComfortFoam 44220
FDA UDI
Class IActive
AquaRite Extra CMC Healogics by DermaRite 93053
FDA UDI
Class IActive
HydraLock SA 60610
FDA UDI
Class IActive
DermaBlue + Foam Transfer 76020218
FDA UDI
UActive
DermaLevin 00285E
FDA UDI
Class IActive
AquaRite Extra CMC 40318
FDA UDI
Class IActive
DermaDress 12410
FDA UDI
Class IActive
StayStrips 72254
FDA UDI
Class IActive
ComfortFoam Border Healogics by DermaRite 93218
FDA UDI
Class IActive
DermaLevin 00285E
FDA UDI
Class IActive
DermaFilm Thin With border 32670
FDA UDI
Class IActive
DermaFilm HD Healogics by DermaRite 93411
FDA UDI
Class IActive
AquaRite Extra CMC 40220
FDA UDI
Class IActive
UnnaRite w/ Zinc Healogics by DermaRite 93971
FDA UDI
Class IActive
DermaFilm X-Thin Clear w/Grid, Oval Healogics by DermaRite 93433
FDA UDI
Class IActive
Oil Emulsion Gauze Dressing 22316
FDA UDI
Class IActive
ComfiTape 69250
FDA UDI
Class IActive
DermaBlue + Foam 76040514
FDA UDI
UActive
Oil Emulsion Dressing 22380
FDA UDI
Class IActive
DermaView II 00254E
FDA UDI
Class IActive
DermaView II Transparent Dressing 16410
FDA UDI
Class IActive
ComfortFoam Healogics by DermaRite 931937
FDA UDI
Class IActive
DermaFilm Thin With border 32670
FDA UDI
Class IActive
DermaBlue + Foam Transfer 76020218
FDA UDI
UActive
ComfiTel 56340
FDA UDI
Class IActive
Petrolatum Gauze Dressing 23180
FDA UDI
Class IActive
ComfortFoam Border 43250
FDA UDI
Class IActive
DermaBlue + Foam 76020214
FDA UDI
UActive
DermaFoam Tracheostomy 45330
FDA UDI
Class IActive
ComfortFoam Border Sacral Healogics by DermaRite 93232
FDA UDI
Class IActive
Oil Emulsion Dressing 22590
FDA UDI
Class IActive
ComfiTel 56230
FDA UDI
Class IActive
Sterile Bordered Gauze 00261E
FDA UDI
Class IActive
DermaView II 00253E
FDA UDI
Class IActive
Sterile Bordered Gauze 00263E
FDA UDI
Class IActive
DermaGinate/Ag 00520E
FDA UDI
UActive
ComfortFoam Border Healogics by DermaRite 93214
FDA UDI
Class IActive
ComfortFoam Border 43412
FDA UDI
Class IActive
DermaFoam Tracheostomy 45330
FDA UDI
Class IActive
ComfortFoam Border Lite 47440
FDA UDI
Class IActive
AquaRite Extra CMC 40318
FDA UDI
Class IActive
DermaFilm X-Thin Clear w/Grid, Oval Healogics by DermaRite 93432
FDA UDI
Class IActive
ComfortFoam/Ag 49450
FDA UDI
UActive
ComfortFoam Border Sacral 43880
FDA UDI
Class IActive
DermaFoam Healogics by DermaRite 93453
FDA UDI
Class IActive
DermaGinate/Ag 00535E
FDA UDI
UActive
DermaDress 00278E
FDA UDI
Class IActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.