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Sign in to claim this brandBG MEDICAL, LLC
US
Last updated May 24, 2026
What BG MEDICAL, LLC makes
BG Medical, LLC produces synthetic polymer surgical mesh designed for extra-gynaecological applications, intended for use in procedures requiring tissue reinforcement or support. The mesh is non-bioabsorbable, meaning it remains in place within the body after implantation.
The company’s products fall under FDA Class II devices and are listed in the FDA’s Unique Device Identification (UDI) database. BG Medical, LLC 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 BG Medical, LLC manufacture?
BG Medical, LLC specializes in producing synthetic polymer surgical mesh intended for extra-gynaecological applications. These devices are designed to reinforce or support tissue during surgical procedures and are non-bioabsorbable, meaning they remain in place within the body after implantation.
Where is BG Medical, LLC based?
BG Medical, LLC is headquartered in the United States. The company’s location is relevant for regulatory compliance and device distribution within the country.
How are BG Medical, LLC’s devices classified by regulatory authorities?
BG Medical, LLC’s devices fall under FDA Class II classification. This classification is assigned based on the level of risk associated with the device, with Class II devices requiring special controls in addition to general controls to ensure safety and effectiveness.
Are BG Medical, LLC’s devices listed in any regulatory registries?
Yes, BG Medical, LLC’s devices are included in the FDA’s Unique Device Identification (UDI) database. The UDI system helps track and trace medical devices throughout their distribution and use, ensuring transparency and accountability in the healthcare system.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 825244135
Catalogue (25)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| SurgiMesh | T4040 | FDA UDI | Class II | Active |
| SurgiMesh | Tintra E-1522 | FDA UDI | Class II | Active |
| SurgiMesh | Tintra R-1415 | FDA UDI | Class II | Active |
| SurgiMesh | T3030 | FDA UDI | Class II | Active |
| SurgiMesh | Tintra O-2636 | FDA UDI | Class II | Active |
| SurgiMesh | T1116-8XD | FDA UDI | Class II | Active |
| SurgiMesh | Tintra CK-7 | FDA UDI | Class II | Active |
| SurgiMesh | TEALFIL-8 | FDA UDI | Class II | Active |
| SurgiMesh | T510 | FDA UDI | Class II | Active |
| SurgiMesh | Tintra OK-1522 | FDA UDI | Class II | Active |
| SurgiMesh | Tintra E-2226 | FDA UDI | Class II | Active |
| SurgiMesh | Tintra C-12 | FDA UDI | Class II | Active |
| SurgiMesh | T1415 | FDA UDI | Class II | Active |
| SurgiMesh | T613-8S | FDA UDI | Class II | Active |
| SurgiMesh | T1418-8XD | FDA UDI | Class II | Active |
| SurgiMesh | TEL613-8 | FDA UDI | Class II | Active |
| SurgiMesh | T1015 | FDA UDI | Class II | Active |
| SurgiMesh | T1115-8 | FDA UDI | Class II | Active |
| SurgiMesh | T5050 | FDA UDI | Class II | Active |
| SurgiMesh | Tintra C-15 | FDA UDI | Class II | Active |
| SurgiMesh | Tintra C-10 | FDA UDI | Class II | Active |
| SurgiMesh | Tintra E-3030 | FDA UDI | Class II | Active |
| SurgiMesh | Tintra CK-10 | FDA UDI | Class II | Active |
| SurgiMesh | T221510 | FDA UDI | Class II | Active |
| SurgiMesh | Tintra OK-1015 | FDA UDI | Class II | Active |
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