Medical Device Manufacturer · US , Mchenry , IL

J. Aderer, Inc. - FDA 510(k) Cleared Devices

24 submissions · 24 cleared · Since 1981

24

Total

24

Cleared

0

Denied

J. Aderer, Inc. has 24 FDA 510(k) cleared dental devices. Based in Mchenry, US.

Historical record: 24 cleared submissions from 1981 to 1982.

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

J. Aderer, 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. Aderer, Inc.

24 devices

1-24 of 24

Cleared Oct 26, 1982

Cleared Oct 26, 1982

Cleared Jul 13, 1982

Cleared Jul 06, 1982

Cleared Jun 14, 1982

Cleared Jun 14, 1982

Cleared Jun 09, 1982

Cleared Jun 09, 1982

Cleared Jun 09, 1982

Cleared Jun 04, 1982

E.G. BRIDGE GOLD

Cleared May 28, 1982

Cleared May 10, 1982

PRECIOUS METAL ALLOYS

Cleared May 05, 1982

Cleared Mar 02, 1982

Cleared Jan 07, 1982

Cleared Jan 07, 1982

Cleared Oct 02, 1981

Cleared Jul 15, 1981

Cleared Apr 14, 1981

Cleared Apr 14, 1981

SR-IVOSEAL(SOFT RELINING)

Cleared Apr 14, 1981

Cleared Apr 14, 1981

Cleared Mar 17, 1981

SR-IVOTRAY SPECIAL

Cleared Mar 17, 1981

SR-IVOTRAY UNIVERSAL