510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K934265Substantially Equivalent

Flexmedics Super-Seven Stranded Nickel-Titanium Archwire

Flexmedics, Minnetonka MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K934265 is the FDA 510(k) clearance record for FLEXMEDICS SUPER-SEVEN STRANDED NICKEL-TITANIUM ARCHWIRE, a class I device, cleared for Flexmedics on under FDA product code DZC (Wire, Orthodontic). FDA records list 20 510(k) clearances for Flexmedics, from to . As of , FDA records show no recalls naming K934265.

Clearance record

Decision date
Received
(143 days to decision)
Product code
DZC Wire, Orthodontic
Regulation
21 CFR 872.5410
Device class
Class I
Review panel
Dental
Applicant
Flexmedics 12400 Whitewater Dr., Suite 2040, Minnetonka MN
510(k) summary
Statement
Third party review
No

Clearances, product code DZC

Trailing 12 months

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

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