Medical Device Manufacturer · US , Mchenry , IL

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

45 submissions · 45 cleared · Since 1979

Recent clearances: BOSWORTH AEGIS LINER & RESTORATIVE MATERIAL W/ACP, BOSWORTH AIR POLISHER, BOSWORTH DENTIN RESIN

45

Total

45

Cleared

0

Denied

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

45 devices

1-12 of 45

Cleared Mar 04, 2011

BOSWORTH AEGIS LINER & RESTORATIVE MATERIAL W/ACP

Cleared Dec 03, 2010

BOSWORTH AIR POLISHER

Cleared Sep 11, 2006

BOSWORTH DENTIN RESIN

Cleared Jul 28, 2005

Cleared Feb 25, 2005

Cleared Mar 19, 2004

AEGIS ORTHO DUAL-CURED ORTHODONTIC ADHESIVE

Cleared Mar 19, 2004

AEGIS ORTHO LIGHT-CURED ORTHODONTIC ADHESIVE

Cleared Feb 05, 2004

AEGIS PIT & FISSURE SEALANT WITH ACP

Cleared Oct 02, 2003

ALGINATE IMPRESSION MATERIAL III (FAST & REGULAR)

Cleared Sep 04, 2003

PIT & FISSURE SEALANT WITH FLUORIDE

Cleared Apr 13, 2000

ACTIVATOR PASTE

Cleared Dec 21, 1999

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

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