Medical Device Manufacturer · US , North Attleborough , MA

Metalor Technologies USA - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2001

Recent clearances: XERAFIT, V-GNATHOS SUPRA, YELLOW SPECIAL

View 4 510(k) Devices ↓

4

Total

4

Cleared

0

Denied

FDA 510(k) Regulatory Record - Metalor Technologies USA Dental ✕

4 devices

1-4 of 4

Cleared Feb 14, 2002

Cleared Jan 22, 2002

V-GNATHOS SUPRA

Cleared Jan 03, 2002

Cleared Dec 19, 2001

Data Source

Sourced from the FDA 510(k) public files . 176,583 total devices indexed.

Last updated: Oct 08, 2026