510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K940785Substantially Equivalent

Mouth Props

Worldwide Dental, Inc., Clearwater FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K940785 is the FDA 510(k) clearance record for MOUTH PROPS, a class I device, cleared for Worldwide Dental, Inc. on under FDA product code EIF (Accessories, Retractor, Dental). FDA records list 4 510(k) clearances for Worldwide Dental, Inc., from to . As of , FDA records show no recalls naming K940785.

Clearance record

Decision date
Received
(225 days to decision)
Product code
EIF Accessories, Retractor, Dental
Regulation
21 CFR 872.4565
Device class
Class I
Review panel
Dental
Applicant
Worldwide Dental, Inc. 12890 Automobile Blvd.,, Clearwater FL
510(k) summary
Statement
Third party review
No

Clearances, product code EIF

Trailing 12 months

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

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