Medical Device Manufacturer · US , Rockville Centre , NY

Metalor - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1994

3

Total

3

Cleared

0

Denied

FDA 510(k) Regulatory Record - Metalor Dental ✕

3 devices

1-3 of 3

Cleared Nov 02, 1994

V-DELTA N (V-DELTA LOY), AUROFLUID 2PF

Cleared Jan 06, 1994

Cleared Jan 06, 1994

Data Source

Sourced from the FDA 510(k) public files . 175,972 total devices indexed.

Last updated: Apr 28, 2026