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Sign in to claim this brandArmstrong Medical Supply, LLC
US
Last updated May 30, 2026
What Armstrong Medical Supply, LLC makes
The company manufactures nitrile examination and treatment gloves that are non-powdered and non-antimicrobial, designed for medical and clinical use. These products include variants such as DEFENDER MAX, DEFENDER PLUS, and DEFENDER, which are intended for protective barrier applications during medical procedures.
These devices are classified under FDA’s Class I regulatory category and are listed in the FDA’s Unique Device Identification (UDI) system. The manufacturer operates within the United States, adhering to applicable U.S. medical device regulations.
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 Armstrong Medical Supply, LLC manufacture?
Armstrong Medical Supply, LLC specializes in nitrile examination and treatment gloves that are non-powdered and non-antimicrobial. These gloves are designed as protective barriers for use in medical and clinical settings, ensuring safety during procedures. Examples include the DEFENDER MAX, DEFENDER PLUS, and DEFENDER series.
Where is Armstrong Medical Supply, LLC based?
The company is based in the United States, where it operates and manufactures its medical devices in compliance with applicable U.S. regulations.
Which regulatory registries or databases list the devices made by Armstrong Medical Supply, LLC?
The devices produced by Armstrong Medical Supply, LLC are listed in the FDA’s Unique Device Identification (UDI) system. This database helps track and identify medical devices authorized for use in the U.S.
How are the devices manufactured by Armstrong Medical Supply, LLC classified by the FDA?
The company’s nitrile examination and treatment gloves fall under the FDA’s Class I regulatory category. Class I devices are generally considered to pose the lowest risk and typically require less regulatory oversight, though they must still meet specific safety and performance standards.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- armstrongmed.com
- —
- —
- [email protected]
- Phone
- 2819709411
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 962708454
Catalogue (18)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Defender Max | AMSDEF6-XS | FDA UDI | Class I | Active |
| Defender Plus | AMSDEF5-XXL | FDA UDI | Class I | Active |
| Defender | AMSDEF4-L | FDA UDI | Class I | Active |
| Defender Max | AMSDEF6-XL | FDA UDI | Class I | Active |
| Defender Max | AMSDEF6-L | FDA UDI | Class I | Active |
| Defender Max | AMSDEF6-S | FDA UDI | Class I | Active |
| Defender Plus | AMSDEF5-M | FDA UDI | Class I | Active |
| Defender Plus | AMSDEF5-XS | FDA UDI | Class I | Active |
| Defender | AMSDEF4-2XL | FDA UDI | Class I | Active |
| Defender | AMSDEF4-S | FDA UDI | Class I | Active |
| Defender | AMSDEF4-M | FDA UDI | Class I | Active |
| Defender Max | AMSDEF6-M | FDA UDI | Class I | Active |
| Defender Plus | AMSDEF5-XL | FDA UDI | Class I | Active |
| Defender Plus | AMSDEF5-L | FDA UDI | Class I | Active |
| Defender Plus | AMSDEF5-S | FDA UDI | Class I | Active |
| Defender | AMSDEF4-XL | FDA UDI | Class I | Active |
| Defender Max | AMSDEF6-XXL | FDA UDI | Class I | Active |
| Defender | AMSDEF4-XS | FDA UDI | Class I | Active |
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