510(k) clearances

CO2 Laser System (MBT- CO2 Laser)

Beijing Mega Beauty Technology Co., Ltd. · General, Plastic Surgery

K262269Substantially EquivalentTraditionalGEX
Open FDA's page for this record
Third party flag
N
City
Beijing
Advisory committee description
General, Plastic Surgery
Address 1
Rm. 1-524, Bldg. #4, Xingyuan Rd. #27, Daxing District
Statement or summary
Summary
Product code
GEX
Zip code
102629
Applicant
Beijing Mega Beauty Technology Co., Ltd.
Decision date
2026-09-01
Decision code
SESE
Country code
CN
Device name
CO2 Laser System (MBT- CO2 Laser)
Advisory committee
SU
Contact
Alex Yu
K number
K262269
Date received
2026-07-06
Review advisory committee
SU
Postal code
102629
Decision description
Substantially Equivalent
Clearance type
Traditional
Harmonized identifiers (openFDA)
Device name
Powered Laser Surgical Instrument
Medical specialty description
General, Plastic Surgery
Regulation number
878.4810
Device class
2
Registration number
3009488834, 3009380063, 3005580113, 3013619029, 3011657089, 3037047060, 3038373471, 3042255006, 3005855240, 3006849754, 3004111573, 3009649442, 3016170453, 3004378299, 1318319, 3003340844, 3043011436, 1222993, 3012322232, 3004633032, 3034456223, 3004374705, 3037966040, 3005791808, 3019906161, 3020900954, 3009383334, 3038197172, 3046005941, 2939653, 3012133441, 3015807001, 3025268687, 1319211, 3007583504, 3021349626, 1037955, 3043012240, 3009887511, 1424785 +452 more
FEI number
3009488834, 3009380063, 3005580113, 3013619029, 3011657089, 3037047060, 3038373471, 3042255006, 3005855240, 3006849754, 3004111573, 3009649442, 3016170453, 3004378299, 1318319, 3003340844, 3043011436, 3012322232, 3004633032, 3034456223, 3004374705, 3037966040, 3005791808, 3019906161, 3020900954, 3009383334, 3003067608, 3000219468, 3038197172, 3046005941, 2939653, 3002900199, 3012133441, 3015807001, 3025268687, 1319211, 3007583504, 3021349626, 1037955, 3043012240 +450 more
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Data from openFDA, FDA's public API. FDA says not to rely on it to make decisions about medical care and to treat every result as unvalidated; confirm against FDA's own record and the product labeling. Not medical or legal advice.