510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K080025Substantially Equivalent

Led.l, Led.m, Led.g, Led.b

Guilin Woodpecker Medical Instrument Co., Ltd, Flintville TN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K080025 is the FDA 510(k) clearance record for LED.L, LED.M, LED.G, LED.B, a class II device, cleared for Guilin Woodpecker Medical Instrument Co., Ltd. on under FDA product code EBZ (Activator, Ultraviolet, For Polymerization). FDA records list 14 510(k) clearances for Guilin Woodpecker Medical Instrument Co., Ltd., from to . As of , FDA records show no recalls naming K080025.

Clearance record

Decision date
Received
(75 days to decision)
Product code
EBZ Activator, Ultraviolet, For Polymerization
Regulation
21 CFR 872.6070
Device class
Class II
Review panel
Dental
Applicant
Guilin Woodpecker Medical Instrument Co., Ltd. 340 Shady Grove Rd., Flintville TN
510(k) summary
Statement
Third party review
Yes

Clearances, product code EBZ

Trailing 12 months
1 clearance under product code EBZ in the twelve months to October 2026, June 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code EBZ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20261
July 20260
August 20260
September 20260
October 20260