Hu-Friedy Mfg. Co., Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Hu-Friedy Mfg. Co., Inc. has 8 FDA 510(k) cleared medical devices. Based in Chicago, US.
Historical record: 8 cleared submissions from 1984 to 2010. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Hu-Friedy Mfg. Co., Inc. Filter by specialty or product code using the sidebar.
8 devices
Cleared
Mar 30, 2010
SWERV MAGNETOSTRICTIVE ULTRASONIC SCALER SYSTEM
Dental
42d
Cleared
Feb 27, 2008
EI DOWNPAK BARRIER SLEEVES
Dental
89d
Cleared
Jun 21, 2007
SYMMETRY IQ, MODEL 2000 SERIES, 3000 SERIES
Dental
76d
Cleared
Feb 01, 2006
SYMMETRY S-SERIES PIEZOELECTRIC SCALING TIPS
Dental
79d
Cleared
Jul 27, 2001
MODIFICATION TO:HU-FRIEDY BRAND SATIN SWIVEL ULTRASONIC INSERT
Dental
25d
Cleared
Oct 07, 1995
DENTAL ULTRASONIC SCALER INSERTS
Dental
47d
Cleared
Jul 24, 1991
ACCU-PLACER TM KIT
Dental
50d
Cleared
Nov 08, 1984
HU-FRIEDY IMS CASSETTE SYSTEM
Radiology
27d