HomeFranceNEWCLIP TECHNICS SAS

NEWCLIP TECHNICS SAS

France · Haute Goulaine Loire-Atlantique
✓ Record-verifiedregistrations found in 3 markets

This company has registrations in United States, Brazil, Canada — 3 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
25listed device types
Class I 22Class II 3Class III 0
plus 55 registration records and 34 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
16registered devices
Class I 7Class II 9
26 including historic records
SASaudi ArabiaSFDA
0registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
0active device licences
3 including historic records
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 States55 registration records, 34 510(k), 0 PMA
Brazil16 confirmed, 0 excluded
Manufacturer names merged into this page: NEWCLIP TECHNICS SAS · NEWCLIP TECHNICS S.A.S.

Company information

Country
France
City
Haute Goulaine Loire-Atlantique

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

22006
12009
12010
12013
12014
22015
32016
52017
42018
12020
22021
12022
12023
22024
32025
42026

FDA listed device types

showing 8 of 25
Screw, Fixation, Bone 1Plate, Fixation, Bone 1Orthopaedic Surgical Planning And Instrument Guides 1Template 1Forceps 1Handle, Scalpel 1Impactor 1Guide, Surgical, Instrument 1

Registration details (sample)

MarketIdentifierNameClass / date
USK261511Xpert Ankle2026-07-28
USK261191Alians Elbow S2026-07-08
USK261038Xpert PFP2026-05-29
BR82684019001Initial R Xpert 2.4 - Template IntraoperatórioClass II
BR82684019002Initial R Xpert 2.4 - Kit de remoçãoClass II
BR82684019003Initial R Xpert 2.4 - Kit InstrumentalClass II

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