510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K261253Substantially Equivalent

Laser Hair Growth Devices (HR-H1, HR-H2, HR-H3, HR-H4, HR-H5, HR-H6, HR-H7, HR-H8, HR-H9, HR-H10, HR-I1, HR-I2, HR-I3, HR-I4, HR-I5)

Ziree Co., Ltd., Changsha, CN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K261253 is the FDA 510(k) clearance record for Laser Hair Growth Devices (HR-H1, HR-H2, HR-H3, HR-H4, HR-H5, HR-H6, HR-H7, HR-H8, HR-H9, HR-H10, HR-I1, HR-I2, HR-I3, HR-I4, HR-I5), a class II device, cleared for Ziree Co., Ltd. on under FDA product code OAP (Laser, Comb, Hair). FDA's definition for product code OAP reads: "Promote hair growth in males with androgenic alopecia and norwood hamilton classification of iia to v". FDA records list one 510(k) clearance for Ziree Co., Ltd. As of , FDA records show no recalls naming K261253.

Clearance record

Decision date
Received
(71 days to decision)
Product code
OAP Laser, Comb, Hair
Regulation
21 CFR 890.5500
Device class
Class II
Review panel
Physical Medicine
Applicant
Ziree Co., Ltd. Rm. 606, Floor 6th, Unit 1, Bldg. 6, Chaoshi Intelligent Ind, Changsha, CN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code OAP

Trailing 12 months
9 clearances under product code OAP in the twelve months to October 2026, June 2026 the highest month at 4.
Show the numbers
Monthly 510(k) clearances under FDA product code OAP, trailing twelve months
MonthClearances
November 20250
December 20251
January 20261
February 20260
March 20260
April 20260
May 20260
June 20264
July 20261
August 20260
September 20262
October 20260