Medical Device Manufacturer · US , Mchenry , IL

Harry J. Bosworth Co. - FDA 510(k) Cleared Devices

45 submissions · 45 cleared · Since 1979

Total

Cleared

Denied

Harry J. Bosworth Co. has 45 FDA 510(k) cleared dental devices. Based in Mchenry, US.

Historical record: 45 cleared submissions from 1979 to 2011.

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

Harry J. Bosworth Co. 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 - Harry J. Bosworth Co.

45 devices

1-12 of 45

Cleared Mar 04, 2011

BOSWORTH AEGIS LINER & RESTORATIVE MATERIAL W/ACP

K103585 · EMA

Dental · 87d

Cleared Dec 03, 2010

BOSWORTH AIR POLISHER

K100731 · EFB

Dental · 263d

Cleared Sep 11, 2006

BOSWORTH DENTIN RESIN

AEGIS ORTHO DUAL-CURED ORTHODONTIC ADHESIVE

K040547 · DYH

Dental · 17d

Cleared Mar 19, 2004

AEGIS ORTHO LIGHT-CURED ORTHODONTIC ADHESIVE

K040548 · DYH

Dental · 17d

Cleared Feb 05, 2004

AEGIS PIT & FISSURE SEALANT WITH ACP

K033751 · EBC

Dental · 66d

Cleared Oct 02, 2003

ALGINATE IMPRESSION MATERIAL III (FAST & REGULAR)

K031439 · ELW

Dental · 149d

Cleared Sep 04, 2003

PIT & FISSURE SEALANT WITH FLUORIDE

PA GEL 35% IN BLUE AND PA GEL 10% IN GREEN OR BLUE

K993716 · EBF

Dental · 49d

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Harry J. Bosworth Co. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Harry J. Bosworth Co.

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