A-dec 54.1073.01
by A-Dec, Inc.
A-dec 54.1073.01 is a Class I device made by A-Dec, Inc., cleared under FDA 510(k) K251811 on 25 Aug 2025 and listed in FDA GUDID since 19 Feb 2026 (UDI-DI 10194665008482), 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 | Number10194665008482 | Date19 Feb 2026 | StatusListed |
| United States | FDA 510(k)SESE | NumberK251811 | Date25 Aug 2025 | StatusActive |
Official records
- AccessGUDID record 10194665008482
- FDA 510(k) database K251811
Across registries
- FDA 510(k) K251811 decided 25 Aug 2025 Active
- FDA GUDID UDI-DI 10194665008482 listed 19 Feb 2026 Listed
Timeline
- Cleared FDA 510(k) K251811
- Listed FDA GUDID 10194665008482
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- A-dec
- Generic name
- Dental surgical power tool motorized handpiece/set, electric
- Model / Ref / Catalog
- 54.1073.01
- Primary DI / UDI-DI
- 10194665008482
- 510(k) Number
- FDA product code
- EBW, EKX, LQY
- GMDN term
- Dental surgical power tool motorized handpiece/set, electric
- Device class
- Class I
- Regulation number
- 872.4200
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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