Schiller Corp.

Switzerland · Baar

✓ Record-verifiedregistrations found in 10 markets

This company has registrations in United States, Brazil, Canada, Taiwan, Singapore, South Korea, Australia, Hong Kong, Israel, Russia — 10 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

15listed device types

Class I 4Class II 10Class III 0unclassified 1

plus 18 registration records and 18 510(k)

UKUnited KingdomMHRA PARD

pendingnot queried

BRBrazilANVISA

3registered devices

Class II 3

4 including historic records

SASaudi ArabiaSFDA

0registered imported devices

low-risk imported devices only; a 2023 snapshot, not updated since

CACanadaMDALL

10active device licences

Class II 7Class III 3

32 including historic records

TWTaiwanTFDA

13valid device licences

Class II 10Class III 3

SGSingaporeHSA SMDR

33device registrations

CLASS B 25CLASS C 8

KRSouth KoreaMFDS GMP

1GMP quality-system certificates

Import 1

AUAustraliaTGA ARTG

17active ARTG entries

Class I 2IIa 11IIb 4

HKHong KongMDACS

1valid listings

Class III 1

ILIsraelAMAR

12registrations

RURussiaRoszdravnadzor

18active registrations

Class 2a 1Class 2b 17

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 States18 registration records, 18 510(k), 0 PMA, 4 excluded

Brazil3 confirmed, 1 excluded

Canada10 confirmed, 1 excluded

Manufacturer names merged into this page: SCHILLER AG · SCHILLER AG.

FDA 510(k) clearances by year

21985

11987

11999

12000

12002

22004

22005

12006

12007

12010

12016

12017

12020

12023

12026

FDA listed device types

showing 8 of 15

Computer, Diagnostic, Programmable 1System, Measurement, Blood-Pressure, Non-Invasive 1Spirometer, Diagnostic 1Dc-Defibrillator, Low-Energy, (Including Paddles) 1Aid, Cardiopulmonary Resuscitation 1Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms) 1Oximeter 1Electrocardiograph 1

Registration details (sample)

Market	Identifier	Name	Class / date
US	K253562	medilogFD	2026-08-14
US	K221056	ARGUS PB-3000	2023-07-06
US	K183425	CARDIOVIT AT-102 G2	2020-03-02
BR	80443699015	Cardiovit	Class II
BR	80443699016	Eletrocardiógrafo	Class II
BR	80011680035	ELETROCARDIÓGRAFO	Class II
CA	17444	WELCH ALLYN/SCHILLER ELECTROCARDIOGRAPHS	Class II
CA	17658	WELCH ALLYN/SCHILLER SPIROMETER	Class II
CA	66345	SCHILLER MONITORING ARGUS LCM	Class III