510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K931329Substantially Equivalent

Dental Instruments Curette Periodontal

Minnesota Prophy Power, Inc., Lakeville MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K931329 is the FDA 510(k) clearance record for DENTAL INSTRUMENTS CURETTE PERIODONTAL, a class I device, cleared for Minnesota Prophy Power, Inc. on under FDA product code EMS (Curette, Periodontic). FDA records list 2 510(k) clearances for Minnesota Prophy Power, Inc., from to . As of , FDA records show no recalls naming K931329.

Clearance record

Decision date
Received
(317 days to decision)
Product code
EMS Curette, Periodontic
Regulation
21 CFR 872.4565
Device class
Class I
Review panel
Dental
Applicant
Minnesota Prophy Power, Inc. 11538 172nd St., Lakeville MN
510(k) summary
Statement
Third party review
No

Clearances, product code EMS

Trailing 12 months

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

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