510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K900809Substantially Equivalent

Lee-Fischer Ceramic Reinforced Plastic Brackets

Lee Pharmaceuticals, South El Monte CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K900809 is the FDA 510(k) clearance record for LEE-FISCHER CERAMIC REINFORCED PLASTIC BRACKETS, a class II device, cleared for Lee Pharmaceuticals on under FDA product code DYW (Bracket, Plastic, Orthodontic). FDA records list 29 510(k) clearances for Lee Pharmaceuticals, from to . As of , FDA records show no recalls naming K900809.

Clearance record

Decision date
Received
(127 days to decision)
Product code
DYW Bracket, Plastic, Orthodontic
Regulation
21 CFR 872.5470
Device class
Class II
Review panel
Dental
Applicant
Lee Pharmaceuticals 1444 Santa Anita, South El Monte CA
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