510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K915717Substantially Equivalent

Cedeta

D-W Intl., Vancouver WA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K915717 is the FDA 510(k) clearance record for CEDETA, cleared for D-W Intl. on under FDA product code LWM (Device, Electrical Dental Anesthesia). FDA records list one 510(k) clearance for D-W Intl. As of , FDA records show no recalls naming K915717.

Clearance record

Decision date
Received
(340 days to decision)
Product code
LWM Device, Electrical Dental Anesthesia
Device class
Unclassified
Review panel
Unknown
Applicant
D-W Intl. 3212 SE 147th Pl., Vancouver WA
510(k) summary
Summary
Third party review
No

Clearances, product code LWM

Trailing 12 months

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

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