510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K242363Substantially Equivalent

HIGHERDOSE Red Light Hat (HG-120K)

Shenzhen Kaiyan Medical Equipment Co., Ltd, Shenzhen, CN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K242363 is the FDA 510(k) clearance record for HIGHERDOSE Red Light Hat (HG-120K), a class II device, cleared for Shenzhen Kaiyan Medical Equipment 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 24 510(k) clearances for Shenzhen Kaiyan Medical Equipment Co., Ltd., from to . As of , FDA records show no recalls naming K242363.

Clearance record

Decision date
Received
(103 days to decision)
Product code
OAP Laser, Comb, Hair
Regulation
21 CFR 890.5500
Device class
Class II
Review panel
Physical Medicine
Applicant
Shenzhen Kaiyan Medical Equipment Co., Ltd. Bldg.#3 And Bldg.#5, 40th Of Fuxin St., Shenzhen, 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