510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K931330Substantially Equivalent

Dental Instruments Scaler

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

K931330 is the FDA 510(k) clearance record for DENTAL INSTRUMENTS SCALER, a class I device, cleared for Minnesota Prophy Power, Inc. on under FDA product code EMN (Scaler, Periodontic). FDA records list 2 510(k) clearances for Minnesota Prophy Power, Inc., from to . As of , FDA records show no recalls naming K931330.

Clearance record

Decision date
Received
(316 days to decision)
Product code
EMN Scaler, 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 EMN

Trailing 12 months

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

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