TensionTac DFX0045R
TensionTac DFX0045R is a Class II device made by Dunamis Medical LLC, listed in FDA GUDID since 11 Aug 2023 (UDI-DI 00854629006987), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00854629006987 | Date11 Aug 2023 | StatusListed |
Official records
- AccessGUDID record 00854629006987
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- TensionTac
- Generic name
- Orthopaedic bone screw, non-bioabsorbable, sterile
- Model / Ref / Catalog
- DFX0045R
- Primary DI / UDI-DI
- 00854629006987
- FDA product code
- MBI
- GMDN term
- Orthopaedic bone screw, non-bioabsorbable, sterile
- Device class
- Class II
- Regulation number
- 888.3040
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Safe
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