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Sign in to claim this brandEssential Medical Supply, Inc.
US
Last updated May 30, 2026
What Essential Medical Supply, Inc. makes
Essential Medical Supply, Inc. manufactures alternating-pressure mattress overlay systems designed to reduce pressure ulcers and improve patient comfort, including bubble pads and pump units. They also produce transcutaneous electrical nerve stimulation (TENS) systems for pain management, including electrode sets and digital TENS devices.
Their products are classified as Class II medical devices under FDA regulations and are listed in the FDA’s 510(k) and Unique Device Identifier (UDI) databases. 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 Essential Medical Supply, Inc. manufacture?
Essential Medical Supply, Inc. manufactures alternating-pressure bed mattress overlay systems, including bubble pads and pump units, designed to reduce pressure ulcers and improve patient comfort. They also produce transcutaneous electrical nerve stimulation (TENS) systems for pain management, including electrode sets and digital TENS devices. These products are based solely on the device categories and examples provided in the data.
Where is Essential Medical Supply, Inc. based?
Essential Medical Supply, Inc. operates from the United States, as explicitly stated in the SUMMARY section of the provided device data. No further details about specific locations, facilities, or headquarters are included in the data, so the answer is limited to the country of operation as given.
In which regulatory registries are Essential Medical Supply, Inc.'s devices listed?
The devices manufactured by Essential Medical Supply, Inc. are listed in the FDA’s 510(k) database and the FDA’s Unique Device Identifier (UDI) database, as indicated in the LISTED IN field of the device data. These are the only registries mentioned, and no other domestic or international registries are referenced in the provided information.
How are Essential Medical Supply, Inc.'s devices classified under FDA regulations?
Essential Medical Supply, Inc.'s devices are classified as Class II medical devices under FDA regulations, as explicitly stated in the DEVICE CLASSES field of the provided data. This classification applies to the alternating-pressure mattress overlay systems and TENS systems described, and no other classifications or device-specific variations are mentioned in the data.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- essentialmedicalsupply.com
- —
- —
- [email protected]
- Phone
- 407-770-0710
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 189331325
Catalogue (18)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Manta | IPN928169 | FDA UDI | Class III | Active |
| Endurance Standard Alternating Pressure Bubble Pad w/Flaps | D8800EX | FDA UDI | Class II | Active |
| Manta | IPN928168 | FDA UDI | Class III | Active |
| Manta | IPN928166 | FDA UDI | Class III | Active |
| Manta | IPN928167 | FDA UDI | Class III | Active |
| MANTA 8F Depth Locator | 188F | FDA UDI | Class III | Active |
| Endurance Standard Alternating Pressure Bubble Pad | D8800 | FDA UDI | Class II | Active |
| Manta | 2156 | FDA UDI | Class III | Active |
| Endurance Deluxe Alternating Pressure Pump | D9000 | FDA UDI | Class II | Active |
| Endurance Deluxe Alternating Pressure Pump & Pad Combo | D9000C | FDA UDI | Class II | Active |
| TENS Electrode Set | S1000E | FDA UDI | Class II | Active |
| Endurance Standard Alternating Pressure Pump | D8000 | FDA UDI | Class II | Active |
| Essential TENS System | S1000 | FDA UDI | Class II | Active |
| Essential Digital TENS System | S2000 | FDA UDI | N/A | Active |
| Endurance Standard Alternating Pressure Pump & Pad Combo | D8000C | FDA UDI | Class II | Active |
| MANTA 14F Depth Locator | 114F | FDA UDI | Class III | Active |
| Manta | 2115 | FDA UDI | Class III | Active |
| Endurance R3000 | K942384 | FDA 510(k) | Class II | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
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Notified Bodies
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Authorities
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FDA Recalls (2)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
Essential Medical Supply, Inc. has two recall records initiated between May 8, 2009, and December 21, 2009, both of which are marked as terminated. The recalls involve the W1801B and W1801R Endurance HD Walkers, citing reports and test findings that the front caster may detach from the frame due to potential plastic fork collapse or stud failure.
AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Dec 21, 2009 | Z-2269-2010 | — | terminated | Essential Medical Supply, Inc. is recalling W1801B and W1801R Endurance HD Walkers due to recent reports and tests that show the front caster may detach from the frame. The potential failures include a collapse of the plastic fork or shearing of the stud attaching the caster to the frame. |
| May 8, 2009 | Z-1674-2009 | — | terminated | The caster may separate from the frame completely causing injury to the user. |