HomeUSARusch, Inc.

Rusch, Inc.

USA · Duluth
✓ Record-verifiedregistrations found in 4 markets

This company has registrations in United States, Brazil, Canada, Singapore — 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
26510(k) clearances
Class I 0Class II 0Class III 0
plus 0 registration records and 26 510(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
1active device licences
Class II 1
3 including historic records
TWTaiwanTFDA
0valid device licences
SGSingaporeHSA SMDR
13device registrations
CLASS B 11CLASS C 2
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, 26 510(k), 0 PMA, 1 excluded
Brazil1 confirmed, 5 excluded
Canada1 confirmed, 2 excluded
Manufacturer names merged into this page: RUSCH INC. · RUSCH INC

Company information

Country
USA
City
Duluth

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

101993
61995
31996
21997
21998
22000
12001

Registration details (sample)

MarketIdentifierNameClass / date
USK010420RUSCH MMG/O'NEIL CATHETER2001-05-09
USK993528RUSCH EMERGENCY MASK2000-05-31
USK993194RUSCH MANUAL RESUSCITATOR BAG2000-03-24
BR10150470123SONDA DE FOLEY SILICONE RUSCHClass II
CA12037CELESTIN PULSION TUBEClass II

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