Medical Device Manufacturer · US , Armonk , NY

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

55 submissions · 55 cleared · Since 1988

Total

Cleared

Denied

J.F. Jelenko & Co., Inc. has 55 FDA 510(k) cleared dental devices. Based in Armonk, US.

Historical record: 55 cleared submissions from 1988 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.

J.F. Jelenko & Co., Inc. 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 - J.F. Jelenko & Co., Inc.

55 devices

1-12 of 55

JEL BIOS 90 (CODE NAME RD-2401)

JEL BIOS 10 (CODE NAME RD-1801)

K993136 · EJT

Dental · 31d

Cleared Oct 21, 1999

JEL BIOS 18 (CODE NAME RD- 1214)

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

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

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