Midmark ADS-1200-001
Midmark ADS-1200-001 is a Class I device made by Midmark Corporation, cleared under FDA 510(k) K251626 on 3 Nov 2025 and listed in FDA GUDID since 20 Feb 2026 (UDI-DI 00841709121883), 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 | Number00841709121883 | Date20 Feb 2026 | StatusListed |
| United States | FDA 510(k)SESE | NumberK251626 | Date3 Nov 2025 | StatusActive |
Official records
- AccessGUDID record 00841709121883
- FDA 510(k) database K251626
Across registries
- FDA 510(k) K251626 decided 3 Nov 2025 Active
- FDA GUDID UDI-DI 00841709121883 listed 20 Feb 2026 Listed
Timeline
- Cleared FDA 510(k) K251626
- Listed FDA GUDID 00841709121883
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- Withdrawn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
- ADS-1200-001
- Primary DI / UDI-DI
- 00841709121883
- 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
- MRI safety
- MR Unsafe
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