510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K771006Substantially Equivalent

Modified Podiatry Products

Dentronix, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K771006 is the FDA 510(k) clearance record for MODIFIED PODIATRY PRODUCTS, a class I device, cleared for Dentronix, Inc. on under FDA product code HTZ (Instrument, Cutting, Orthopedic). FDA records list 9 510(k) clearances for Dentronix, Inc., from to . As of , FDA records show no recalls naming K771006.

Clearance record

Decision date
Received
(15 days to decision)
Product code
HTZ Instrument, Cutting, Orthopedic
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Dentronix, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code HTZ

Trailing 12 months

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

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