Medical Device Manufacturer · US , Tampa , FL

Dabi-Atlante America Corp. - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 1991

4

Total

4

Cleared

0

Denied

FDA 510(k) Regulatory Record - Dabi-Atlante America Corp. Dental ✕

4 devices

1-4 of 4

Cleared Mar 04, 1994

HANDPIECE MODELS: MS-350

Cleared Mar 04, 1994

Cleared Dec 21, 1992

HANDPIECE MODELS MS-350, RS-350

Cleared Oct 30, 1991

MINIFLEX AND PERSONAL UNIT

Data Source

Sourced from the FDA 510(k) public files . 175,218 total devices indexed.

Last updated: Apr 27, 2026