Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K964863Substantially Equivalent

Model 45E Handengine & Controller, Model 45Eh Handengine & Controller, Model Rx-100 Handengine & Controller, Model Eteln

Bell Intl., Inc., Burlingame CA / Traditional, Substantially Equivalent

K964863 is the FDA 510(k) clearance record for MODEL 45E HANDENGINE & CONTROLLER, MODEL 45EH HANDENGINE & CONTROLLER, MODEL RX-100 HANDENGINE & CONTROLLER, MODEL ETELN, a class I device, cleared for Bell Intl., Inc. on under FDA product code EBW (Controller, Foot, Handpiece And Cord). FDA records list 2 510(k) clearances for Bell Intl., Inc., from to . As of , FDA records show no recalls naming K964863.

Clearance record

Decision date
Received
(86 days to decision)
Product code
EBW Controller, Foot, Handpiece And Cord
Regulation
21 CFR 872.4200
Device class
Class I
Review panel
Dental
Applicant
Bell Intl., Inc. 31 Edwards Ct., Burlingame CA
510(k) summary
Summary
Third party review
No

Clearances, product code EBW

Trailing 12 months
2 clearances under product code EBW in the twelve months to October 2026, January 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code EBW, trailing twelve months
MonthClearances
November 20250
December 20250
January 20262
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260