HomeStryker Instrument

Stryker Instrument

✓ Record-verifiedregistrations found in 3 markets

This company has registrations in United States, Brazil, Saudi Arabia — 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
110listed device types
Class I 53Class II 56Class III 0unclassified 1
plus 203 registration records and 74 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
16registered devices
Class I 3Class II 13
this export covers Class I / II only (the cadastro route)
SASaudi ArabiaSFDA
195registered 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 States203 registration records, 74 510(k), 0 PMA, 77 excluded
Brazil16 confirmed, 23 excluded
Saudi Arabia195 confirmed, 8 excluded
Canada0 confirmed, 16 excluded
Manufacturer names merged into this page: Stryker Instruments · Stryker Orthmed (Changzhou) Medical Instrument Co., Ltd. · STRYKER INSTRUMENTS · Stryker Instrument

Company information

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

31995
31996
31997
11998
51999
32000
72001
42002
92003
42004
62005
42006
12007
12017
12021
22022
12023
42024
82025
32026

FDA listed device types

showing 8 of 110
Electrosurgical, Cutting & Coagulation & Accessories 1Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component 1Apparatus, Suction, Ward Use, Portable, Ac-Powered 1Thoracolumbosacral Pedicle Screw System 1Electrosurgical, Cutting & Coagulation & Accessories, For Cardiac Electrophysiology Device Implantation And Revision 1Needle, Conduction, Anesthetic (W/Wo Introducer) 1Bottle, Collection, Vacuum 1Apparatus, Suction, Operating-Room, Wall Vacuum Powered 1

Registration details (sample)

MarketIdentifierNameClass / date
USK261544Hydro Irrigation System2026-06-17
USK253679Hydro Irrigation System2026-05-08
USK252282SurgiCount+ System2026-03-16
BR80005430220GORRO FLYTEClass I
BR80005439050bonevacClass II
BR80005430228RECIPIENTE DE ASPIRAÇÃO PARA SONOPETClass I
SAME0000009223SFDAA00001Stryker System G™ Sterilization Case
SAME0000003208SFDAA00387System 6™

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