Medical Device Manufacturer · US , Armonk , NY

J.F. Jelenko & Co., Inc. - FDA 510(k) Cleared Devices

55 submissions · 55 cleared · Since 1988

55

Total

55

Cleared

0

Denied

FDA 510(k) Regulatory Record - J.F. Jelenko & Co., Inc. Dental ✕

55 devices

1-12 of 55

Cleared Aug 22, 2001

Cleared Nov 16, 2000

Cleared Oct 19, 2000

Cleared Aug 31, 2000

Cleared Jun 20, 2000

Cleared May 17, 2000

Cleared May 11, 2000

JEL BIOS 90 (CODE NAME RD-2401)

Cleared Apr 06, 2000

Cleared Oct 21, 1999

JEL BIOS 10 (CODE NAME RD-1801)

Cleared Oct 21, 1999

JEL BIOS 18 (CODE NAME RD- 1214)

Cleared Jun 23, 1999

Cleared Mar 25, 1999

JELDENT MULTICRYL

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