510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K923067Substantially Equivalent

Sens-a-Ray

Regam Medical Systems, V7r 2g2 Canada, CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K923067 is the FDA 510(k) clearance record for SENS-A-RAY, a class II device, cleared for Regam Medical Systems on under FDA product code EHD (Unit, X-Ray, Extraoral With Timer). FDA records list one 510(k) clearance for Regam Medical Systems. As of , FDA records show no recalls naming K923067.

Clearance record

Decision date
Received
(155 days to decision)
Product code
EHD Unit, X-Ray, Extraoral With Timer
Regulation
21 CFR 872.1800
Device class
Class II
Review panel
Dental
Applicant
Regam Medical Systems 631 Monytoyal Blvd., V7r 2g2 Canada, CA
510(k) summary
Statement
Third party review
No

Clearances, product code EHD

Trailing 12 months
6 clearances under product code EHD in the twelve months to October 2026, February 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code EHD, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20262
March 20262
April 20260
May 20261
June 20260
July 20260
August 20260
September 20261
October 20260