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MIDMARK CORPORATION

USA · Orchard Park

✓ Record-verifiedregistrations found in 5 markets

This company has registrations in United States, Saudi Arabia, Canada, Australia, Israel — 5 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

23listed device types

Class I 14Class II 9Class III 0

plus 26 registration records and 39 510(k)

UKUnited KingdomMHRA PARD

pendingnot queried

BRBrazilANVISA

0registered devices

this export covers Class I / II only (the cadastro route)

SASaudi ArabiaSFDA

9registered imported devices

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

CACanadaMDALL

26active device licences

Class II 25Class III 1

64 including historic records

TWTaiwanTFDA

0valid device licences

SGSingaporeHSA SMDR

pendingnot queried

KRSouth KoreaMFDS GMP

pendingnot queried

AUAustraliaTGA ARTG

2active ARTG entries

Class I 1IIb 1

HKHong KongMDACS

pendingnot queried

ILIsraelAMAR

4registrations

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 States26 registration records, 39 510(k), 0 PMA, 1 excluded

Saudi Arabia9 confirmed, 0 excluded

Canada26 confirmed, 0 excluded

Manufacturer names merged into this page: MIDMARK CORPORATION · MIDMARK CORP. · MIDMARK · Midmark Corporation

FDA 510(k) clearances by year

11985

51989

21990

21991

11992

21993

41994

11999

22000

12003

22009

12011

12012

12013

12016

12017

12020

12024

12025

12026

FDA listed device types

showing 8 of 23

Chair, Surgical, Ac-Powered 1Stand, Infusion 1Unit, Operative Dental 1Restraint, Protective 1Unit, Operative Dental, Accessories 1Light, Operating, Dental 1Unit, Suction Operatory 1Scale, Patient 1

Registration details (sample)

Market	Identifier	Name	Class / date
US	K253196	Midmark 800 Digital Vital Signs Device (1-300-0100, 1-300-0200, 1-300-0300, 1-300-0400)	2026-06-12
US	K251626	Midmark Dental Delivery System	2025-11-03
US	K233026	Midmark Smart M9® Sterilizer, Midmark Smart M11® Sterilizer	2024-04-04
SA	ME0000004641SFDAA00001	641-00X	—
SA	ME0000004641SFDAA00002	230-00X	—
CA	5255	EMERGENCY SUCTION UNIT	Class II
CA	6276	NITRONOX ANALGESIA DELIVERY SYSTEM	Class II
CA	64086	HOPE 5 RESUSCITATOR	Class II

MIDMARK CORPORATION

Registrations by market

How these numbers were verified

Company information

FDA 510(k) clearances by year

FDA listed device types

Registration details (sample)

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