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BROWNMED, INC.

United States·US-MF-000008271

Last updated May 23, 2026

What BROWNMED, INC. makes

BrownMed, Inc. manufactures reusable orthopedic and therapeutic devices, including hand and finger splints, waterproof bathing covers for casts and bandages, prefabricated orthotic insoles, ankle/foot orthoses, and suspension arm slings. Their product line also includes reusable hot/cold therapy packs, heel protectors, and hand-held vibration therapy units designed for circulatory and musculoskeletal support.

The company’s devices are classified under Class I and Class II regulations, with listings in the EU’s EUDAMED database and the FDA’s Unique Device Identifier (UDI) system. The manufacturer operates from the United States.

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 BrownMed, Inc. manufacture?

BrownMed, Inc. specializes in reusable orthopedic and therapeutic devices. Their product line includes hand and finger splints for immobilization, waterproof bathing covers for casts and bandages to allow safe water exposure, prefabricated orthotic insoles for arch support, ankle/foot orthoses for alignment or cushioning, and suspension arm slings for shoulder support. They also produce reusable hot/cold therapy packs, heel protectors for pressure relief, and hand-held vibration therapy units targeting circulatory and musculoskeletal conditions.

Where is BrownMed, Inc. based, and how does that affect its devices?

BrownMed, Inc. is based in the United States. This location influences regulatory compliance, as their devices are listed in the FDA’s Unique Device Identifier (UDI) system, ensuring traceability and reporting requirements under U.S. regulations. Additionally, their products are also documented in the EU’s EUDAMED database, indicating their availability or distribution in the European market, though the company itself is not subject to EU regulatory approvals.

Which regulatory registries list BrownMed, Inc.’s devices?

BrownMed, Inc.’s devices are listed in two key regulatory registries: the EUDAMED database, which tracks medical devices marketed in the European Union, and the FDA’s Unique Device Identifier (UDI) system, which ensures device traceability and compliance in the United States. These listings help healthcare providers and regulators identify and verify the devices’ regulatory status.

How are BrownMed, Inc.’s devices classified under medical regulations?

BrownMed, Inc.’s devices fall under Class I and Class II classifications. Class I devices generally pose minimal risk and require general controls (e.g., good manufacturing practices), while Class II devices involve a higher level of risk and may require additional performance standards or post-market surveillance. The classification determines the regulatory scrutiny and labeling requirements for each product.

Why do some of BrownMed’s devices require special care, like waterproofing or reusability?

Several of BrownMed’s devices are designed for reusability (e.g., splints, bathing covers, and therapy packs) to reduce waste and cost for patients and healthcare systems. The waterproof bathing covers for casts and bandages are specifically engineered to allow patients to safely bathe or swim without damaging the immobilization, which is critical for maintaining hygiene and preventing infections. These features align with practical patient needs while adhering to regulatory standards for reusable medical devices.

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

Information

Country
United States
Address
1300, Lundberg Drive West, Spirit Lake, United States
Website
brownmed.com
LinkedIn
—
Facebook
—
Phone
—
PRRC Contact
Brandon Rodriguez
EUDAMED SRN
US-MF-000008271
FDA FEI Number
—
DUNS Number
091999771

Catalogue (432)

Page 3 of 9
DeviceModel / ReferenceRegistriesClassStatus
Seal-Tight 20106
EUDAMEDFDA UDI
Class IActive
Polar Ice 30013
EUDAMEDFDA UDI
Class IActive
Soft Stride 71406
FDA UDI
Class IActive
Nice Stretch 51032
FDA UDI
Class IActive
Imak Rsi A30137
FDA UDI
Class IActive
Soft Stride 71356
EUDAMEDFDA UDI
Class IActive
Spark 40412
EUDAMEDFDA UDI
Class IActive
Nice Stretch 50311
EUDAMEDFDA UDI
Class IActive
Seal-Tight 26503
EUDAMEDFDA UDI
Class IActive
Seal-Tight 29404
EUDAMEDFDA UDI
Class IActive
Intellinetix 07240
FDA UDI
Class IActive
Seal-Tight 29410
FDA UDI
Class IActive
Seal-Tight 20201
EUDAMEDFDA UDI
Class IActive
Plastalume 10702
EUDAMEDFDA UDI
Class IActive
Nice Stretch 52061
FDA UDI
Class IActive
Nice Stretch 53105
EUDAMEDFDA UDI
Class IActive
Plastalume 12123
FDA UDI
Class IActive
Joslin J62538
FDA UDI
Class IActive
Polar Ice 30012
EUDAMEDFDA UDI
Class IActive
Plastalume SP10416-25
FDA UDI
Class IActive
Polar Ice 30107
EUDAMEDFDA UDI
Class IActive
Plastalume 10327
EUDAMEDFDA UDI
Class IActive
Plastalume 10004
EUDAMEDFDA UDI
Class IActive
Spark 40420
FDA UDI
Class IActive
Soft Stride 71362
EUDAMEDFDA UDI
Class IActive
Imak Rsi A20111
FDA UDI
Class IActive
Soft Stride 71366
EUDAMEDFDA UDI
Class IActive
Plastalume 10706
EUDAMEDFDA UDI
Class IActive
Plastalune SP10438-25
FDA UDI
Class IActive
Plastalume 10735
EUDAMEDFDA UDI
Class IActive
Steady Step 50052
EUDAMEDFDA UDI
Class IActive
Soft Stride 71432
FDA UDI
Class IActive
NuRoo 08005
FDA UDI
Class IUnknown
Plastalume 15021
FDA UDI
Class IActive
Spark 40410
FDA UDI
Class IActive
Nice Stretch 51022
FDA UDI
Class IActive
Soft Stride 71424
EUDAMEDFDA UDI
Class IActive
Plastalume 11031
EUDAMEDFDA UDI
Class IActive
Spark 40427
EUDAMEDFDA UDI
Class IActive
Soft Stride 71411
EUDAMEDFDA UDI
Class IActive
Joslin J50101ZL
FDA UDI
Class IActive
Soft Stride 71421
FDA UDI
Class IActive
NuRoo 08281
FDA UDI
Class IUnknown
Imak Rsi A10172
EUDAMEDFDA UDI
Class IActive
Joslin J63538
FDA UDI
Class IActive
Polar Ice 30108
EUDAMEDFDA UDI
Class IActive
Plastalume 10652
EUDAMEDFDA UDI
Class IActive
Imak Rsi A20126
FDA UDI
Class IActive
Seal-Tight 20202
EUDAMEDFDA UDI
Class IActive
NuRoo 08282
FDA UDI
Class IUnknown

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