Kentron 739925
Kentron 739925 is a Class II device made by Kentron Health Care, Inc., cleared under FDA 510(k) K140228 on 18 Dec 2014 and listed in FDA GUDID since 27 May 2026 (UDI-DI 00810003750402), active as of 22 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 | Number00810003750402 | Date27 May 2026 | StatusListed |
| United States | FDA 510(k)SESE | NumberK140228 | Date18 Dec 2014 | StatusActive |
Official records
- AccessGUDID record 00810003750402
- FDA 510(k) database K140228
Across registries
- FDA 510(k) K140228 decided 18 Dec 2014 Active
- FDA GUDID UDI-DI 00810003750402 listed 27 May 2026 Listed
Timeline
- Cleared FDA 510(k) K140228
- Listed FDA GUDID 00810003750402
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Kentron
- Generic name
- Basic endotracheal tube, single-use
- Model / reference
- 739925
- Primary DI / UDI-DI
- 00810003750402
- 510(k) Number
- FDA product code
- BTR
- GMDN term
- Basic endotracheal tube, single-use
- Device class
- Class II
- Regulation number
- 868.5730
- GUDID distribution status
- In Commercial Distribution