510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K931725Substantially Equivalent

Alpha II

Dynarad Corp., Deer Park NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K931725 is the FDA 510(k) clearance record for ALPHA II, a class II device, cleared for Dynarad Corp. on under FDA product code EHD (Unit, X-Ray, Extraoral With Timer). FDA records list 9 510(k) clearances for Dynarad Corp., from to . As of , FDA records show no recalls naming K931725.

Clearance record

Decision date
Received
(100 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
Dynarad Corp. 19 Jefryn Blvd. W., Deer Park NY
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