← FDA DEVICE PRODUCT CODES

FDA PRODUCT CODE · CLASS II

OAPLaser, Comb, Hair

Promote hair growth in males with androgenic alopecia and norwood hamilton classification of iia to v

DEVICE CLASS
Class II
REGULATION
21 CFR 890.5500
MEDICAL SPECIALTY
Physical Medicine
REVIEW PANEL
SU
ImplantLife-sustainingGMP-exemptThird-party review eligible
18
510(K)/PMA CLEARANCES
510k: 18
0
RECALL ENTRIES

Recent clearances

K261675Shenzhen Chuanghong Zhilian Technology Co., Ltd. · 510k2026-07-17
K261253Ziree Co., Ltd. · 510k2026-06-26
K260899Zdeer Technology (Henan) Co., Ltd. · 510k2026-06-16
K253231Hubei Yjt Technology Co.,Ltd · 510k2026-06-16
K251684Alma Lasers, Inc. · 510k2026-06-05
K253669Shenzhen Kaiyan Medical Equipment Co., Ltd. · 510k2026-01-23
K253349Light Tree Ventures Europe B.V. · 510k2025-12-24
K252414Shenzhen Kaiyan Medical Equipment Co., Ltd. · 510k2025-10-30

Related on SPEQ

Medical devices industryMedical device quality (ISO 13485)FDA device clearancesFDA enforcement & recalls

Source: FDA device classification, 510(k)/PMA, and recall datasets (openFDA). Recall entries count distinct FDA recall numbers, so one recall event affecting several products appears as several entries. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data.

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