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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 2 of 9
DeviceModel / ReferenceRegistriesClassStatus
Nice Stretch 50088
FDA UDI
Class IActive
Steady Step 50145
FDA UDI
Class IActive
Plastalume 10707
EUDAMEDFDA UDI
Class IActive
Soft Stride 71361
EUDAMEDFDA UDI
Class IActive
Plastalume 10021
EUDAMEDFDA UDI
Class IActive
Plastalume 10501
FDA UDI
Class IActive
Plastalume 10323
EUDAMEDFDA UDI
Class IActive
Seal-Tight 20100
EUDAMEDFDA UDI
Class IActive
Imak Rsi A30141A30140
FDA UDI
Class IActive
Plastalume 12131
FDA UDI
Class IActive
Seal-Tight 20200
FDA UDI
Class IActive
Seal-Tight 20324
EUDAMEDFDA UDI
Class IActive
Seal-Tight 29413
FDA UDI
Class IActive
Seal Tight 20435
EUDAMEDFDA UDI
Class IActive
IMAK Compression A20187
FDA UDI
Class IActive
Imak Rsi A10301
FDA UDI
Class IActive
Plastalume 10105
EUDAMEDFDA UDI
Class IIActive
Seal-Tight 29403
EUDAMEDFDA UDI
Class IActive
Plastalume 12423
FDA UDI
Class IActive
Plastalume SP10417-25
FDA UDI
Class IActive
Plastalume SP10441-25
FDA UDI
Class IActive
Plastalume 12113
FDA UDI
Class IActive
Polar Ice A10303
EUDAMEDFDA UDI
Class IActive
Imak Rsi 60000
FDA UDI
Class IActive
Seal-Tight 29408
FDA UDI
Class IActive
Polar Ice A10304
EUDAMEDFDA UDI
Class IActive
Seal-Tight 20363
EUDAMEDFDA UDI
Class IActive
Steady Step 50041
EUDAMEDFDA UDI
Class IActive
Plastalume 10624
EUDAMEDFDA UDI
Class IActive
Intellinetix 07237
FDA UDI
Class IActive
Seal-Tight 20107
EUDAMEDFDA UDI
Class IActive
Seal-Tight 20103
EUDAMEDFDA UDI
Class IActive
Polar Ice 30103
EUDAMEDFDA UDI
Class IActive
Plastalume 11121
EUDAMEDFDA UDI
Class IActive
Joslin J50201ZL
FDA UDI
Class IActive
Plastalume 15031
FDA UDI
Class IActive
Plastalume 10003
EUDAMEDFDA UDI
Class IActive
Imak Rsi A20161
FDA UDI
Class IActive
Plastalume 10705
EUDAMEDFDA UDI
Class IActive
Nice Stretch 51033
FDA UDI
Class IActive
Steady Step 50053
EUDAMEDFDA UDI
Class IActive
Plastalume 12513
FDA UDI
Class IActive
Seal-Tight 20326
EUDAMEDFDA UDI
Class IActive
Plastalume 10621
EUDAMEDFDA UDI
Class IActive
Plastalume 12033
FDA UDI
Class IActive
Joslin J50601ZL
FDA UDI
Class IActive
Seal-Tight 20362
EUDAMEDFDA UDI
Class IActive
Soft Stride 71435
FDA UDI
Class IActive
Intellinetix 07236
FDA UDI
Class IActive
Soft Stride 71381
FDA UDI
Class IActive

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