510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K872622Substantially Equivalent

Orthodontic Arch

Wonder Wire, Wyomissing PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K872622 is the FDA 510(k) clearance record for ORTHODONTIC ARCH, a class I device, cleared for Wonder Wire on under FDA product code EJZ (Knife, Margin Finishing, Operative). FDA records list 2 510(k) clearances for Wonder Wire, from to . As of , FDA records show no recalls naming K872622.

Clearance record

Decision date
Received
(95 days to decision)
Product code
EJZ Knife, Margin Finishing, Operative
Regulation
21 CFR 872.4565
Device class
Class I
Review panel
Dental
Applicant
Wonder Wire P.O. Box 6499, Wyomissing PA
Third party review
No

Clearances, product code EJZ

Trailing 12 months

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

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