510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K883120Substantially Equivalent

Flex Plastic Plastic Coated Nitinol Arch Wire

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

K883120 is the FDA 510(k) clearance record for FLEX PLASTIC PLASTIC COATED NITINOL ARCH WIRE, a class I device, cleared for Flexmedics on under FDA product code EJF (Bracket, Metal, Orthodontic). FDA records list 20 510(k) clearances for Flexmedics, from to . As of , FDA records show no recalls naming K883120.

Clearance record

Decision date
Received
(111 days to decision)
Product code
EJF Bracket, Metal, Orthodontic
Regulation
21 CFR 872.5410
Device class
Class I
Review panel
Dental
Applicant
Flexmedics 620 Ford Ctr., 420 N. Fifth, Minneapolis MN
Third party review
No

Clearances, product code EJF

Trailing 12 months

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

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