Parkell, Inc. - FDA 510(k) Cleared Devices
53
Total
53
Cleared
0
Denied
Parkell, Inc. has 53 FDA 510(k) cleared dental devices. Based in Mchenry, US.
Latest FDA clearance: Aug 2025. Active since 1976.
Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Parkell, Inc.
53 devices
Cleared
Aug 08, 2025
Parkell Pit and Fissure Sealant
Dental
297d
Cleared
Jan 20, 2022
Parkell Self-Adhesive Cement
Dental
353d
Cleared
Nov 22, 2019
Parkell Desensitizer Gel
Dental
211d
Cleared
Sep 05, 2019
SmarTemp X1
Dental
148d
Cleared
Dec 14, 2018
HyperFil-LV
Dental
112d
Cleared
Nov 21, 2017
Parkell Universal Adhesive
Dental
125d
Cleared
Sep 18, 2015
BRUSH&BOND PLUS
Dental
105d
Cleared
Feb 24, 2015
EAZY PRIMER
Dental
147d
Cleared
Jun 25, 2014
ABSOLUTE DENTIN 2
Dental
351d
Cleared
Apr 12, 2012
RETRACT GINGIVAL RETRACTION/HEMOSTATIC PASTE
Dental
106d
Cleared
Jun 10, 2010
RETRIEVE IMPLANT CEMENT
Dental
57d
Cleared
May 13, 2008
DURAFINISH ALL-CURE, MODEL S296
Dental
76d
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