HomeFranceBiom'Up Sas

Biom'Up Sas

France · Saint-Priest
✓ Record-verifiedregistrations found in 5 markets

This company has registrations in United States, Canada, Australia, Israel, Russia — 5 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
2510(k) clearances
Class I 0Class II 0Class III 0
plus 0 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
0registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
2active device licences
Class IV 2
TWTaiwanTFDA
0valid device licences
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
1active ARTG entries
IIa 1
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
1registrations
RURussiaRoszdravnadzor
1active registrations
Class 3 1
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 States0 registration records, 2 510(k), 0 PMA
Brazil0 confirmed, 1 excluded
Canada2 confirmed, 0 excluded
Manufacturer names merged into this page: BIOM'UP SA

Company information

Country
France
City
Saint-Priest

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

12011 · K103087
12012 · K103081

Registration details (sample)

MarketIdentifierNameClass / date
USK103081COVAORTHO-NERVE RESORBABLE COLLAGEN MEMBRANE2012-03-02
USK103087COVAMAX RESORBABLE COLLAGEN MEMBRANE2011-08-26
CA91963MATRI BONEClass IV
CA93124COVA COLLAGEN GUIDED HEALING MEMBRANEClass IV

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