KOJ — Airbrush Class II

FDA Device Classification

FDA product code KOJ covers "Airbrush", a Class II medical device regulated under 21 CFR 872.6080. Submissions are reviewed by the Dental panel. At least 20 recent 510(k) clearances have been granted under this product code.

Classification details

Product Code
KOJ
Device Class
Class II
Regulation Number
872.6080
Submission Type
510(k)
Review Panel
DE
Medical Specialty
Dental
Implant
No

Recent 510(k) clearances

K-NumberApplicantDevice NameDate
K251425Mectronturbodent touchMay 9, 2025
K063236Brainbase CorporationBETA-POWDERFeb 16, 2007
K042872Kavo America CorporationRONDOFLEX PLUS 360Nov 23, 2004
K033675Sirona Dental SystemsPROSMILE AIR POLISHER AND PROPHYLAXIS POWDERJan 15, 2004
K033215Danville MaterialsPREPAIRJan 9, 2004
K024105Velopex InternationalVELOPEX AQUACUT FLUID ABRASION UNITOct 9, 2003
K030292GromanGROMAN PREPMASTERApr 15, 2003
K0214503M Espe Ag Dental ProductsCLINPRO PROPHY POWDERAug 1, 2002
K014188Dentsply IntlNEW PROPHY POWDERMar 15, 2002
K014252DeldentJETSTREAMFeb 19, 2002
K014249DeldentJETPOLISHERFeb 19, 2002
K014245DeldentJETSONIC 2000Jan 29, 2002
K013969DeldentMINIBLASTERJan 10, 2002
K984380Kis ProductsDISPO ETCHAug 6, 2001
K993124Kis ProductsDISPODRILLAug 6, 2001
K993182Kis ProductsDISPOPROPHYAug 6, 2001
K010816RonvigDENTO-PREP PARTICLE MICROBLASTERMay 10, 2001
K002708Kavo AmericaKAVO CORUND HANDPIECE 2013Nov 28, 2000
K990060KreativMACH 7Jun 15, 2000
K001313Air TechnologiesAIRDENT II CSJun 8, 2000

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.