Medical Device Manufacturer · US , Edina , MN

Imcor - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1996

7

Total

7

Cleared

0

Denied

Imcor has 7 FDA 510(k) cleared medical devices. Based in Edina, US.

Historical record: 7 cleared submissions from 1996 to 1999. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by Imcor Filter by specialty or product code using the sidebar.

Imcor 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 - Imcor

7 devices

1-7 of 7

Cleared Nov 01, 1999

ALTIVA CORPORATION NTR 3.3 MM SELF-TAPPING SCREW IMPLANTS, ALTIVA CORPORATION...

Cleared Jan 11, 1999

IMCOR 4.00 & 5.00MM SELF-TAPPING LOCKTITE IMPLANTS, IMCOR 4.00 & 5.00MM...

Cleared Oct 15, 1998

IMCOR DENTAL IMPLANT SYSTEM ACCESSORIES

Cleared Jan 30, 1998

IMCOR 3.75 AND 5.00MM EXTERNALLY HEXED, SELF TAPPING HA COATED SCREW IMPLANTS...

Cleared Nov 13, 1997

IMCOR EXTERNALLY HEXED, SELF-TAPPING SCREW IMPLANT SURGICAL DRILLING SYSTEM

Cleared Jun 17, 1996

IMCOR 5.00 MM HEX SELF-TAPPING SCREW W/COVER SCREW

Cleared Jun 05, 1996

IMCOR 3.75 MM WIDE HEX SELF-TAPPING SCREW W/COVER SCREW