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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 7 of 9
DeviceModel / ReferenceRegistriesClassStatus
DermaLevin 00280E
FDA UDI
Class IActive
StayStrips 72251
FDA UDI
Class IActive
Flexpress 4 79000
FDA UDI
Class IActive
DermaView II Island Healogics by DermaRite 93674
FDA UDI
Class IActive
ComfortFoam Border Healogics by DermaRite 93212
FDA UDI
Class IActive
DermaDress 00278E
FDA UDI
Class IActive
DermaFoam Healogics by DermaRite 93452
FDA UDI
Class IActive
DermaView Transparent Film Roll 15411
FDA UDI
Class IActive
Hydralock SA Healogics by DermaRite 93794
FDA UDI
Class IActive
SilvaKollagen Gel 00500
FDA UDI
UUnknown
DermaGinate 00275E
FDA UDI
Class IActive
ComfortFoam Border Healogics by DermaRite 93216
FDA UDI
Class IActive
Silk Tape 501221
FDA UDI
Class IActive
HydraLock SA 60770
FDA UDI
Class IActive
StayStrips 72540
FDA UDI
Class IActive
ComfortFoam Border Lite 47440
FDA UDI
Class IActive
Bordered Foam 00288E
FDA UDI
Class IActive
HydraFoam 00294E
FDA UDI
Class IActive
ComfortFoam Border Lite 47330
FDA UDI
Class IActive
Sterile Bordered Gauze Healogics by DermaRite 93137
FDA UDI
Class IActive
DermFilm HD 00239E
FDA UDI
Class IActive
ComfortFoam 00316E
FDA UDI
Class IActive
HydraLock SA 60610
FDA UDI
Class IActive
ComfortFoam/Ag 49660
FDA UDI
UActive
Sterile Bordered Gauze 11364
FDA UDI
Class IActive
DermaLevin Healogics by DermaRite 93551
FDA UDI
Class IActive
DermaGinate 00270E
FDA UDI
Class IActive
DermaBlue + Foam 76020214
FDA UDI
UActive
DermaFoam Healogics by DermaRite 93451
FDA UDI
Class IActive
ComfortFoam Border Lite Healogics by DermaRite 93251
FDA UDI
Class IActive
DermaDress 12414
FDA UDI
Class IActive
DermaFilm X-Thin Clear with Grid 31460
FDA UDI
Class IActive
DermaCol Healogics by DermaRite 93311
FDA UDI
UActive
Sterile Bordered Gauze Healogics by DermaRite 93133
FDA UDI
Class IActive
DermaView II Island Dressing 16660
FDA UDI
Class IActive
Bordered Foam 4" Round 00288E
FDA UDI
Class IActive
DermaCol 00303E
FDA UDI
UActive
Bordered Foam 00297E
FDA UDI
Class IActive
UnnaRite 78310Z
FDA UDI
Class IActive
DermaBlue + Foam Transfer 76040518
FDA UDI
UUnknown
ComfortFoam/Ag Healogics by DermaRite 93273
FDA UDI
UActive
DermaBlue + Foam 75081614
FDA UDI
UActive
ComfortFoam/Ag Border 48660
FDA UDI
UActive
ComfortFoam Border Sacral Healogics by DermaRite 93233
FDA UDI
Class IActive
DermaBlue + Foam 76040514
FDA UDI
UUnknown
FlexPress 2 79202
FDA UDI
Class IActive
Sterile Bordered Gauze 00262E
FDA UDI
Class IActive
Sterile Bordered Gauze Healogics by DermaRite 93135
FDA UDI
Class IActive
DermaView II 00252E
FDA UDI
Class IActive
ComfortFoam 44330
FDA UDI
Class IActive

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