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Sign in to claim this brandEncompass Group, L.L.C.
US
Last updated May 27, 2026
What Encompass Group, L.L.C. makes
Encompass Group, L.L.C. manufactures reusable patient surgical drapes, single-use and reusable patient gowns, hypothermia-prevention whole-body suits, reusable sterilization packaging, reusable surgical gowns, laboratory aprons, and reusable basic bed sheets.
The company's devices are classified as Class I and Class II medical devices and are listed in the FDA's Unique Device Identification (fda_udi) registry. The company is based in 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 Encompass Group, L.L.C. manufacture?
Encompass Group, L.L.C. manufactures reusable patient surgical drapes, single-use and reusable patient gowns, hypothermia-prevention whole-body suits, reusable sterilization packaging, reusable surgical gowns, laboratory aprons, and reusable basic bed sheets. These products are designed for use in healthcare settings to support infection control, patient comfort, and thermal regulation during medical procedures.
Where is Encompass Group, L.L.C. based?
Encompass Group, L.L.C. is based in the United States. This information is provided directly in the device data summary, which states the company's country as US, indicating its primary operational and legal jurisdiction is within the United States.
In which regulatory registry are Encompass Group, L.L.C.'s devices listed?
Encompass Group, L.L.C.'s devices are listed in the FDA's Unique Device Identification (fda_udi) registry. This registry is maintained by the U.S. Food and Drug Administration to track and identify medical devices through a standardized system, and the company's inclusion confirms its devices are registered for U.S. market distribution under this framework.
How are Encompass Group, L.L.C.'s devices classified under regulatory standards?
Encompass Group, L.L.C.'s devices are classified as Class I and Class II medical devices. This classification reflects the level of regulatory control required to ensure safety and effectiveness, with Class I devices subject to general controls and Class II devices requiring additional special controls such as performance standards or post-market surveillance, based on their intended use and risk profile.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- encompassgroup.net
- —
- —
- [email protected]
- Phone
- 770-626-2167
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 121788819
Catalogue (298)
Page 3 of 6| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Encompass | CD0355 | FDA UDI | Class II | Active |
| Encompass | 30118-224 | FDA UDI | Class II | Active |
| Encompass | 45799-304 | FDA UDI | Class I | Active |
| Encompass | CD1105 | FDA UDI | Class II | Active |
| Thermoflect | 5140-400 | FDA UDI | Class I | Active |
| Encompass | 45790-012 | FDA UDI | Class I | Active |
| Encompass | 45799-102 | FDA UDI | Class I | Active |
| Encompass | CD0244 | FDA UDI | Class II | Active |
| Encompass | CD0956 | FDA UDI | Class II | Active |
| Encompass | 45772-608 | FDA UDI | Class I | Active |
| Encompass | CD1120 | FDA UDI | Class II | Active |
| Encompass | 48003 | FDA UDI | Class I | Active |
| Encompass | 45772-304 | FDA UDI | Class I | Active |
| Thermoflect | 5000-840 | FDA UDI | Class I | Active |
| Thermoflect | 5000-800 | FDA UDI | Class I | Active |
| Encompass | 26182-054 | FDA UDI | Class II | Active |
| Encompass | 30118-232S | FDA UDI | Class II | Active |
| Encompass | 49416-210 | FDA UDI | Class I | Active |
| Encompass | 45410-103 | FDA UDI | Class I | Active |
| Thermoflect | 5400-230 | FDA UDI | Class I | Active |
| Encompass | 26186-572 | FDA UDI | Class II | Active |
| Encompass | 4910 | FDA UDI | Class I | Active |
| Encompass | P9166 | FDA UDI | Class I | Active |
| Thermoflect | 5190-600 | FDA UDI | Class I | Active |
| Encompass | 46722-117 | FDA UDI | Class II | Active |
| Encompass | CD0459 | FDA UDI | Class I | Active |
| Encompass | 45790-104 | FDA UDI | Class I | Active |
| Encompass | 30124-002 | FDA UDI | Class II | Active |
| Encompass | 46150-066 | FDA UDI | Class I | Active |
| Encompass | G-P9164 | FDA UDI | Class I | Active |
| Encompass | 50035-290 | FDA UDI | Class I | Active |
| Thermoflect | 5140-250 | FDA UDI | Class I | Active |
| Encompass | VA550-25XB | FDA UDI | Class II | Active |
| Encompass | 26186-054 | FDA UDI | Class II | Active |
| Encompass | 46722-119 | FDA UDI | Class II | Active |
| Encompass | 26182-012 | FDA UDI | Class II | Active |
| Encompass | 45897-VROS | FDA UDI | Class I | Active |
| Encompass | 45751-102 | FDA UDI | Class I | Active |
| Encompass | CD1102 | FDA UDI | Class II | Active |
| Thermoflect | 5190-500 | FDA UDI | Class I | Active |
| Encompass | G-P9152 | FDA UDI | Class I | Active |
| Encompass | 26182-036 | FDA UDI | Class II | Active |
| Airisana | ARSN--4280 | FDA UDI | Class II | Active |
| Encompass | G-P9154 | FDA UDI | Class I | Active |
| Encompass | 26183-054 | FDA UDI | Class II | Active |
| Encompass | 45202-3XL | FDA UDI | Class I | Active |
| Encompass | CD0903 | FDA UDI | Class II | Active |
| Encompass | G-P9155 | FDA UDI | Class I | Active |
| Thermoflect | 5140-600 | FDA UDI | Class I | Active |
| Encompass | CD1113 | FDA UDI | Class II | Active |
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