HomeUSACOVIDIEN, anteriormente registrada como United States Surgical, a division of Tyco Healthc

COVIDIEN, anteriormente registrada como United States Surgical, a division of Tyco Healthc

USA
✓ Record-verifiedregistrations found in 2 markets

This company has registrations in United States, Brazil — 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
218510(k) clearances
Class I 0Class II 0Class III 0
plus 0 registration records and 218 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
1registered devices
Class II 1
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
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 States0 registration records, 218 510(k), 0 PMA
Brazil1 confirmed, 0 excluded
Manufacturer names merged into this page: COVIDIEN, anteriormente registrada como United States Surgical, a division of Tyco Healthc

Company information

Country
USA

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

21988
71989
241990
161991
91992
111993
321994
171995
151996
131997
131998
81999
52000
62001
32002
32003
22004
12005
42006
22007

Registration details (sample)

MarketIdentifierNameClass / date
USK071406AUTOSUTURE ENDO CLIP III 5 MM CLIP APPLIER2007-11-21
USK071920AUTOSUTURE ABSORBABLE TACK AND APPLICATOR2007-09-28
USK061288AUTO SUTURE ENDO CLIP III 5 MM CLIP APPLIER2006-11-02
BR10349000311GRAMPEADOR MULTIUSO RELIAMAXClass II

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