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 3 of 9
DeviceModel / ReferenceRegistriesClassStatus
DermaCol 100 Healogics by DermaRite 93331
FDA UDI
UActive
ComfortFoam 44480
FDA UDI
Class IActive
DermaSyn/Ag 00510
FDA UDI
UActive
DermaView II Island Dressing 16660
FDA UDI
Class IActive
ComfortGauze Border 42262
FDA UDI
Class IActive
Bordered Foam 00297E
FDA UDI
Class IActive
DermaView II Transparent Dressing 16812
FDA UDI
Class IActive
DermaView Transparent Dressing 15611
FDA UDI
Class IActive
DermaCol 00303E
FDA UDI
UActive
AquaRite Ag Extra CMC 46450
FDA UDI
Class IUnknown
Sterile Bordered Gauze 00261E
FDA UDI
Class IActive
ComfortFoam Border Lite 47220
FDA UDI
Class IActive
ComfortFoam/Ag Border 48660
FDA UDI
UActive
Oil Emulsion Dressing 22590
FDA UDI
Class IActive
DermaBlue + Foam 72040414
FDA UDI
UActive
ComfortFoam Border 00318E
FDA UDI
Class IActive
DermaBlue + Foam 76040414
FDA UDI
UActive
DermaView IV Transparent Dressing 15230IV
FDA UDI
Class IActive
DermaView II Island 16340
FDA UDI
Class IActive
Bordered Foam Healogics by DermaRite 93071
FDA UDI
Class IActive
DermaBlue + Foam 72040414
FDA UDI
UActive
Xerofrom Gauze Healogics by DermaRite 94012
FDA UDI
Class IActive
StayStrips 72253
FDA UDI
Class IActive
DermaView II Island Dressing 16220
FDA UDI
Class IActive
Bordered Foam Healogics by DermaRite 93073
FDA UDI
Class IActive
StingFree Pad 00237
FDA UDI
Class IActive
Bordered Foam 4" Round 00288E
FDA UDI
Class IActive
Sterile Bordered Gauze Healogics by DermaRite 93134
FDA UDI
Class IActive
ComfortFoam Border 43412
FDA UDI
Class IActive
Sting Free 00236
FDA UDI
Class IActive
DermaFilm Sacral 00279E
FDA UDI
Class IActive
Petrolatum Gauze Dressing 23180
FDA UDI
Class IActive
Sterile Bordered Gauze Healogics by DermaRite 93136
FDA UDI
Class IActive
DermaGauze 00240E
FDA UDI
Class IActive
AquaDerm 00324E
FDA UDI
Class IActive
ComfortFoam Healogics by DermaRite 93196
FDA UDI
Class IActive
ComfortFoam/Ag 49450
FDA UDI
UActive
DermaBlue + Foam Transfer 76040418
FDA UDI
UUnknown
Silk Tape 501211
FDA UDI
Class IActive
DermaCol 00302E
FDA UDI
UActive
Petrolatum Gauze Dressing 23390
FDA UDI
Class IActive
DermaFoam Heel/ Elbow Healogics by DermaRite 93454
FDA UDI
Class IActive
ComfortFoam Border 43770
FDA UDI
Class IActive
ComfortFoam Border 43680
FDA UDI
Class IActive
ComfortFoam/Ag 49220
FDA UDI
UActive
Xeroform Gauze Dressing 24220
FDA UDI
Class IActive
ComfortFoam Healogics by DermaRite 93193
FDA UDI
Class IActive
DermaBlue + Foam 76040414
FDA UDI
UActive
UnnaRite C 78310ZC
FDA UDI
Class IActive
ComfortFoam Border 43220
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.