510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K933455Substantially Equivalent

Computed Oral Radiology System

Schick Technologies, Inc., Sound Beach NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K933455 is the FDA 510(k) clearance record for COMPUTED ORAL RADIOLOGY SYSTEM, a class II device, cleared for Schick Technologies, Inc. on under FDA product code EAP (Unit, X-Ray, Intraoral). FDA records list 13 510(k) clearances for Schick Technologies, Inc., from to . As of , FDA records show no recalls naming K933455.

Clearance record

Decision date
Received
(201 days to decision)
Product code
EAP Unit, X-Ray, Intraoral
Regulation
21 CFR 872.1810
Device class
Class II
Review panel
Dental
Applicant
Schick Technologies, Inc. 30 Northport Rd., Sound Beach NY
510(k) summary
Statement
Third party review
No

Clearances, product code EAP

Trailing 12 months

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

FDA records show no clearances under product code EAP in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code EAP, 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