HomeItalyCitieffe S.R.L.

Citieffe S.R.L.

Italy · Calderara Di Reno
✓ Record-verifiedregistrations found in 5 markets

This company has registrations in United States, Brazil, 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
8510(k) clearances
Class I 0Class II 0Class III 0
plus 0 registration records and 8 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
27registered devices
Class I 25Class II 2
35 including historic records
SASaudi ArabiaSFDA
0registered 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
2active ARTG entries
IIb 2
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
1registrations
RURussiaRoszdravnadzor
2active registrations
Class 2b 2
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, 8 510(k), 0 PMA, 2 excluded
Brazil27 confirmed, 0 excluded
Manufacturer names merged into this page: CITIEFFE S.R.L · CITIEFFE S.R.L.

Company information

Country
Italy
City
Calderara Di Reno

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

12013
12014
12015
12017
12018
22019
12025

Registration details (sample)

MarketIdentifierNameClass / date
USK250197Estremo Fibular Nail2025-10-17
USK183666EBA One Nailing System2019-11-14
USK181540Estremo Citieffe Nailing System2019-01-16
BR80203020069Limitador para Fixador Externo CotoveloClass I
BR80203020070Instrumental CitieffeClass I
BR80203029006Instrumental citieffeClass II

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