Medical Device Manufacturer · US , Mchenry , IL

Union Broach, Div. Moyco Industries, Inc. - FDA 510(k) Cleared Devices

14 submissions · 14 cleared · Since 1982

Total

Cleared

Denied

Union Broach, Div. Moyco Industries, Inc. has 14 FDA 510(k) cleared dental devices. Based in Mchenry, US.

Historical record: 14 cleared submissions from 1982 to 1996.

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

Union Broach, Div. Moyco Industries, 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 - Union Broach, Div. Moyco Industries, Inc.

14 devices

1-12 of 14

Cleared Oct 11, 1996

CYBER-FIL ALKENOATE CEMENT MULTI-PURPOSE KIT (23900/23905/23910/23915/23920)

NICKEL-TITANIUM K-TYPE FILE

General Hospital · 90d

Cleared Apr 13, 1990

UNION BROACH BLEACHING LIGHT

K895174 · EEG

Dental · 249d

Cleared Mar 06, 1986

FLEXOR FLEXIBLE ROANE TIP ENDODONTIC FILE

K855136 · EKS

Dental · 73d

Cleared Jul 01, 1985

UNION BROACH BLEACHING LIGHT

K852474

Dental · 20d

Cleared Dec 15, 1982

ENDODONTIC BROACH-BARBED BROACH

K823489 · EKW

Dental · 22d

Cleared Sep 28, 1982

ROOT CANAL REAMERS, TYPE K

K822620 · EKP

Dental · 29d

Union Broach, Div. Moyco Industries, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Union Broach, Div. Moyco Industries, Inc.

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