Midmark 153740-012
Midmark 153740-012 is a Class I device made by Midmark Corporation, cleared under FDA 510(k) K003090 on 18 Oct 2000 and listed in FDA GUDID since 11 Mar 2026 (UDI-DI 00841709122156), 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 | Number00841709122156 | Date11 Mar 2026 | StatusListed |
| United States | FDA 510(k)SESE | NumberK003090 | Date18 Oct 2000 | StatusActive |
Official records
- AccessGUDID record 00841709122156
- FDA 510(k) database K003090
Across registries
- FDA 510(k) K003090 decided 18 Oct 2000 Active
- FDA GUDID UDI-DI 00841709122156 listed 11 Mar 2026 Listed
Timeline
- Cleared FDA 510(k) K003090
- Listed FDA GUDID 00841709122156
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Midmark
- Generic name
- Dental delivery system instrument unit, electric
- Model / Ref / Catalog
- 153740-012
- Primary DI / UDI-DI
- 00841709122156
- 510(k) Number
- FDA product code
- EIA
- GMDN term
- Dental delivery system instrument unit, electric
- Device class
- Class I
- Regulation number
- 872.6640
- GUDID distribution status
- In Commercial Distribution
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