Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K934881Substantially Equivalent

Reflections

Cdb Corp., Wilmington NC / Traditional, Substantially Equivalent

K934881 is the FDA 510(k) clearance record for REFLECTIONS, a class I device, cleared for Cdb Corp. on under FDA product code EJF (Bracket, Metal, Orthodontic). FDA records list 2 510(k) clearances for Cdb Corp., from to . As of , FDA records show no recalls naming K934881.

Clearance record

Decision date
Received
(112 days to decision)
Product code
EJF Bracket, Metal, Orthodontic
Regulation
21 CFR 872.5410
Device class
Class I
Review panel
Dental
Applicant
Cdb Corp. 3625 Hwy. 421 N., Wilmington NC
510(k) summary
Statement
Third party review
No

Clearances, product code EJF

Trailing 12 months

FDA records hold no clearances under product code EJF in the trailing twelve months.

FDA records show no clearances under product code EJF in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code EJF, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260