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Sign in to claim this brandPRO MEDICAL SUPPLIES, INC.
US
Last updated May 24, 2026
What PRO MEDICAL SUPPLIES, INC. makes
Pro Medical Supplies, Inc. manufactures single-use transcutaneous electrical stimulation electrodes, electric heating pads for localized body warmth, and handheld electric massagers designed for therapeutic use.
Their products are regulated under FDA Class I and Class II classifications, with some devices listed in the FDA’s 510(k) and UDI registries. The company 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 Pro Medical Supplies, Inc. manufacture?
Pro Medical Supplies, Inc. specializes in three primary categories of therapeutic devices: single-use transcutaneous electrical stimulation electrodes (like StimPatch or ProPatch), electric pads designed for localized body heating (such as ProMed or EcoPatch), and handheld electric massagers (e.g., ProM-555 or PM-355). These products are intended for medical or therapeutic use, often to relieve pain, reduce inflammation, or improve circulation.
Where is Pro Medical Supplies, Inc. based, and how does that affect its devices?
Pro Medical Supplies, Inc. is based in the United States. Since the company operates within the U.S., its devices are subject to FDA regulations, including classification under FDA’s risk-based system (Class I or Class II). This means their products must comply with U.S. medical device standards and may appear in registries like the FDA’s 510(k) database or UDI (Unique Device Identification) system if applicable.
Which regulatory registries list devices from Pro Medical Supplies, Inc., and why?
Some devices from Pro Medical Supplies, Inc. are listed in the FDA’s 510(k) premarket notification registry and the UDI system. The 510(k) registry includes devices deemed substantially equivalent to predicate devices, requiring FDA review before commercialization. The UDI system ensures traceability and transparency in the supply chain by assigning unique identifiers to medical devices, aiding tracking and compliance. Listing in these registries depends on the device’s classification and regulatory pathway.
How are Pro Medical Supplies, Inc.’s devices classified by the FDA, and what does that mean?
Pro Medical Supplies, Inc.’s devices are classified under FDA’s Class I or Class II categories. Class I devices pose minimal risk and typically require general controls (e.g., labeling, manufacturing practices) for compliance. Class II devices involve moderate risk and may require additional controls, such as performance standards or post-market surveillance. The classification determines the regulatory scrutiny and requirements each device must meet before authorization.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- promedspecialties.com
- —
- —
- [email protected]
- Phone
- 215-938-0200
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 135741127
Catalogue (104)
Page 2 of 3| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Baxter | Baxter-022 | FDA UDI | Class II | Active |
| StimPatch | Stim-025 | FDA UDI | Class II | Active |
| ProPatch | ProM-025 | FDA UDI | Class II | Active |
| ProPatch | ProM-021 | FDA UDI | Class II | Active |
| ProPatch | ProM-010 | FDA UDI | Class II | Active |
| ProPatch | ProM-020 | FDA UDI | Class II | Active |
| FlexPlus | ProM-039 | FDA UDI | Class II | Active |
| Gental Patch | ProM-027 | FDA UDI | Class II | Active |
| StimPatch | Stim-030 | FDA UDI | Class II | Active |
| ProMed | ProM-054B | FDA UDI | Class II | Active |
| StimPatch | Stim-025 | FDA UDI | Class II | Active |
| ProPatch | ProM-020 | FDA UDI | Class II | Active |
| ProPatch | ProM-032 | FDA UDI | Class II | Active |
| ProM-500 | ProM-500 | FDA UDI | Class II | Active |
| ProPatch | ProM-024 | FDA UDI | Class II | Active |
| ProM-200 | ProM-200 | FDA UDI | Class II | Active |
| ProM-200 | ProM-200 | FDA UDI | Class II | Active |
| StimPatch | Stim-021 | FDA UDI | Class II | Active |
| FlexPlus | ProM-028 | FDA UDI | Class II | Active |
| ProPatch | ProM-037 | FDA UDI | Class II | Active |
| FlexPlus | ProM-029 | FDA UDI | Class II | Active |
| StimPatch | Stim-021 | FDA UDI | Class II | Active |
| StimPatch | Stim-020 | FDA UDI | Class II | Active |
| EcoPatch | Eco-020 | FDA UDI | Class II | Active |
| ProMed | ProM-053B | FDA UDI | Class II | Active |
| ProPatch | ProM-033 | FDA UDI | Class II | Active |
| Gentle Patch | ProM-034 | FDA UDI | Class II | Active |
| ProM-100 | ProM-100 | FDA UDI | Class II | Active |
| ProPatch | ProM-030 | FDA UDI | Class II | Active |
| ProM-300 | ProM-300 | FDA UDI | Class II | Active |
| StimPatch | Stim-020 | FDA UDI | Class II | Active |
| EcoPatch | Eco-021 | FDA UDI | Class II | Active |
| StimPatch | Stim-021 | FDA UDI | Class II | Active |
| ProPatch | ProM-032 | FDA UDI | Class II | Active |
| ProMed | ProM-053B | FDA UDI | Class II | Active |
| EcoPatch | Eco-030 | FDA UDI | Class II | Active |
| StimPatch | Stim-030 | FDA UDI | Class II | Active |
| ProM-100 | ProM-100 | FDA UDI | Class II | Active |
| ProPatch | ProM-025 | FDA UDI | Class II | Active |
| ProPatch | ProM-036 | FDA UDI | Class II | Active |
| Flex Plus | ProM-022 | FDA UDI | Class II | Active |
| EcoPatch | Eco-030 | FDA UDI | Class II | Active |
| Pm-720 | PM-720 | FDA UDI | Class II | Active |
| Pm-360 | PM-360 | FDA UDI | Class II | Active |
| ProPatch-Kit | ProM-013-Kit | FDA UDI | Class II | Active |
| Ca-020 | CA-020 | FDA UDI | Class II | Active |
| ProPatch | ProM-021 | FDA UDI | Class II | Active |
| Pm-750 | PM-750 | FDA UDI | Class I | Active |
| StimPatch | Stim-025 | FDA UDI | Class II | Active |
| Pro-Med | ProM-054R | FDA UDI | Class II | Unknown |
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