HomeUSAMebo Life Science, Inc.

Mebo Life Science, Inc.

USA · Brea
✓ Record-verifiedregistrations found in 2 markets

This company has registrations in United States, Saudi Arabia — 2 overseas markets. The China NMPA lookup is still pending.

Registrations by market

Each market counts a different unit; figures are not directly comparable
CNChinaNMPA
n/aThis registry lists domestic registrants only
EUEuropean UnionEUDAMED
pendingnot queried
USUnited StatesFDA openFDA
1listed device types
Class I 0Class II 0Class III 0unclassified 1
plus 2 registration records and 2 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
0registered devices
this export covers Class I / II only (the cadastro route)
SASaudi ArabiaSFDA
2registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
0active device licences
TWTaiwanTFDA
pendingnot queried
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
pendingnot queried
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
pendingnot queried
RURussiaRoszdravnadzor
pendingnot queried
Not yet connected: India CDSCO, Indonesia Kemenkes. The public search for Japan PMDA and Vietnam IMDA does not return manufacturer names, so entries cannot be linked to companies coming — where there is no data it is shown as "pending", never estimated.

How these numbers were verified

record-verified

Company-name search in every official database is a substring match and returns same-named but different companies. Each figure below is the count after re-checking every record against the manufacturer name.

United States2 registration records, 2 510(k), 0 PMA
Saudi Arabia2 confirmed, 0 excluded
Manufacturer names merged into this page: SHANGHAI MEBO LIFE SCIENCE & TECHNOLOGY CO., LTD. · MEBO LIFE SCIENCE INCORPORATION · Shanghai MEBO Life Science & Technology Co., Ltd

Company information

Country
USA
City
Brea

Fields marked "pending" have not been obtained yet; that does not mean they do not exist. Risk records (litigation, penalties, operating anomalies) are kept internal and not published.

FDA 510(k) clearances by year

12020 · K193439
12022 · K222657

FDA listed device types

Dressing, Wound, Drug 1

Registration details (sample)

MarketIdentifierNameClass / date
USK222657MEBO Wound Dressing2022-10-18
USK193439MEBO Wound Dressing2020-09-04
SAME0000013475SFDAA00001MEBO
SAME0000013475SFDAA00001MEBO

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