MicroP Dental A002
by Microp Technology (Taiwan), Inc.
MicroP Dental A002 is a dental power tool system handpiece (FDA Class I; FDA product code EFB, Handpiece, Air-Powered, Dental) made by Microp Technology (Taiwan), Inc., cleared under FDA 510(k) K173943 on 24 Jul 2018 and listed in FDA GUDID since 1 Aug 2020 (UDI-DI 04719880151028), 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 | Number04719880151028 | Date1 Aug 2020 | StatusListed |
| United States | FDA 510(k)SESE | NumberK173943 | Date24 Jul 2018 | StatusActive |
Official records
- AccessGUDID record 04719880151028
- FDA 510(k) database K173943
Across registries
- FDA 510(k) K173943 decided 24 Jul 2018 Active
- FDA GUDID UDI-DI 04719880151028 listed 1 Aug 2020 Listed
Timeline
- Cleared FDA 510(k) K173943
- Listed FDA GUDID 04719880151028
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- MicroP Dental
- Generic name
- Dental power tool system handpiece, pneumatic
- Model / reference
- A002
- Primary DI / UDI-DI
- 04719880151028
- 510(k) Number
- FDA product code
- EFB
- GMDN term
- Dental power tool system handpiece, pneumatic
- 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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