Medical Device Manufacturer · US , Rockville Centre , NY

Metalor Dental USA Corp. - FDA 510(k) Cleared Devices

67 submissions · 67 cleared · Since 1991

Total

Cleared

Denied

Metalor Dental USA Corp. has 67 FDA 510(k) cleared dental devices. Based in Rockville Centre, US.

Historical record: 67 cleared submissions from 1991 to 2001.

Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.

Metalor Dental USA Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Metalor Dental USA Corp.

67 devices

1-12 of 67

AUROFLUID M, ALLOY NO. 5315

K993475 · EJS

Dental · 56d

Cleared Dec 08, 1999

V-DELTA SPECIAL, ALLOY NO. 5154

K993505 · EJS

Dental · 54d

Cleared Dec 08, 1999

PAGALINOR 4 , ALLOY NO. 5440

K993506 · EJS

Dental · 54d

Cleared Dec 06, 1999

V-SUPRAGOLD, ALLOY NO. 5024

K993507 · EJT

Dental · 52d

Cleared Dec 06, 1999

V-SUPRA PLUS, ALLOY NO. 5025

K993508 · EJT

Dental · 52d

Cleared Dec 02, 1999

DELTAPAL, ALLOY NO. 5161

Looking for a specific device from Metalor Dental USA Corp.? Search by device name or K-number.

Search all Metalor Dental USA Corp. devices

Metalor Dental USA Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Metalor Dental USA Corp.

Filters