510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K150702Substantially Equivalent

Exceed Tx

Great Lakes Orthodontics, Ltd., Tonawanda NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K150702 is the FDA 510(k) clearance record for Exceed Tx, a class II device, cleared for Great Lakes Orthodontics, Ltd. on under FDA product code DYW (Bracket, Plastic, Orthodontic). FDA records list 13 510(k) clearances for Great Lakes Orthodontics, Ltd., from to . As of , FDA records show no recalls naming K150702.

Clearance record

Decision date
Received
(372 days to decision)
Product code
DYW Bracket, Plastic, Orthodontic
Regulation
21 CFR 872.5470
Device class
Class II
Review panel
Dental
Applicant
Great Lakes Orthodontics, Ltd. 200 Cooper Ave., Tonawanda NY
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DYW

Trailing 12 months
1 clearance under product code DYW in the twelve months to October 2026, November 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code DYW, trailing twelve months
MonthClearances
November 20251
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260