510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K041385Substantially Equivalent

Modification to Computed Oral Radiology System

Schick Technologies, Inc., Long Island City NY / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K041385 is the FDA 510(k) clearance record for MODIFICATION TO 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 K041385.

Clearance record

Decision date
Received
(13 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. 30-00 47th Ave., Long Island City NY
510(k) summary
Summary PDF
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