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Home›USA›Tusker Medical, Inc.

Tusker Medical, Inc.

USA · Austin
✓ Record-verifiedregistrations found in 2 markets

This company has registrations in United States, Canada — 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
2listed device types
Class I 0Class II 1Class III 1
plus 2 registration records and 2 510(k), 12 PMA
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
0registered devices
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
2active device licences
Class II 1Class III 1
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 States2 registration records, 2 510(k), 12 PMA
Canada2 confirmed, 0 excluded
Manufacturer names merged into this page: Tusker Medical Inc. · TUSKER MEDICAL, INC., A SUBSIDIARY OF SMITH & NEPHEW

Company information

Country
USA
City
Austin

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

12017 · K171239
12026 · K252436

FDA listed device types

Tube, Tympanostomy 1Tympanostomy Tube Delivery Product With Drug 1

Registration details (sample)

MarketIdentifierNameClass / date
USK252436Tula Tympanostomy Tube Delivery Device2026-04-23
USK171239TULA Tube Delivery System2017-06-28
CA93272TULA IONTOPHORESIS SYSTEMClass II
CA94427TULA TUBE DELIVERY SYSTEMClass III

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