EF1 Dne-6000-040
EF1 Dne-6000-040 is a Class II device made by Medshape, Inc., cleared under FDA 510(k) K113106 on 4 Jan 2012 and listed in FDA GUDID since 1 Apr 2026 (UDI-DI 00190446914563), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00190446914563 | Date1 Apr 2026 | StatusListed |
| United States | FDA 510(k)SESE | NumberK113106 | Date4 Jan 2012 | StatusActive |
Official records
- AccessGUDID record 00190446914563
- FDA 510(k) database K113106
Across registries
- FDA 510(k) K113106 decided 4 Jan 2012 Active
- FDA GUDID UDI-DI 00190446914563 listed 1 Apr 2026 Listed
Timeline
- Cleared FDA 510(k) K113106
- Listed FDA GUDID 00190446914563
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- EF1
- Generic name
- External orthopaedic fixation system noninvasive component, single-use
- Model / reference
- DNE-6000-040
- Primary DI / UDI-DI
- 00190446914563
- 510(k) Number
- FDA product code
- KTT
- GMDN term
- External orthopaedic fixation system noninvasive component, single-use
- Device class
- Class II
- Regulation number
- 888.3030
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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