HomeFranceProteor SAS

Proteor SAS

France · Dijon Cedex Cote-D'Or
✓ Record-verifiedregistrations found in 4 markets

This company has registrations in United States, Saudi Arabia, Taiwan, Australia — 4 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
7listed device types
Class I 6Class II 1Class III 0
plus 7 registration records and 0 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
0registered devices
this export covers Class I / II only (the cadastro route)
SASaudi ArabiaSFDA
9registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
0active device licences
TWTaiwanTFDA
1valid device licences
Class I 1
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
1active ARTG entries
Class I 1
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 States7 registration records, 0 510(k), 0 PMA, 2 excluded
Brazil0 confirmed, 1 excluded
Saudi Arabia9 confirmed, 0 excluded
Manufacturer names merged into this page: PROTEOR · Proteor SAS

Company information

Country
France
City
Dijon Cedex Cote-D'Or

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 listed device types

Bandage, Cast 1Component, External, Limb, Ankle/Foot 1Prosthesis, Thigh Socket, External Component 1Joint, Knee, External Limb Component 1Joint, Ankle, External Brace 1Valve, Prosthesis 1Assembly, Knee/Shank/Ankle/Foot, External 1

Registration details (sample)

MarketIdentifierNameClass / date
SAME0000021035SFDAA00001DYNACITY
SAME0000021582SFDAA00001HYDEAL II

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