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Kap Medical Corporation

✓ Record-verifiedregistrations found in 6 markets

This company has registrations in United States, United Kingdom, Saudi Arabia, Canada, Australia, Israel — 6 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

0UDI-DI device records

USUnited StatesFDA openFDA

7listed device types

Class I 2Class II 5Class III 0

plus 7 registration records and 0 510(k)

UKUnited KingdomMHRA PARD

1registered device records

Class I 1

BRBrazilANVISA

0registered devices

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

SASaudi ArabiaSFDA

3registered imported devices

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

CACanadaMDALL

0active device licences

3 including historic records

TWTaiwanTFDA

0valid device licences

SGSingaporeHSA SMDR

pendingnot queried

KRSouth KoreaMFDS GMP

pendingnot queried

AUAustraliaTGA ARTG

2active ARTG entries

Class I 2

HKHong KongMDACS

pendingnot queried

ILIsraelAMAR

1registrations

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.

European Union619 raw hits, 300 excluded, 0 confirmed. Large result set — only the first 300 verified

United States7 registration records, 0 510(k), 0 PMA

United Kingdom1 confirmed, 4 excluded

Saudi Arabia3 confirmed, 0 excluded

Manufacturer names merged into this page: KAP MEDICAL · KAP Medical

Regulatory identity

UK responsible person: Obelis UK Ltd

FDA listed device types

Cover, Mattress (Medical Purposes) 1Mattress, Flotation Therapy, Non-Powered 1Bed, Patient Rotation, Powered 1Bed, Ac-Powered Adjustable Hospital 1Mattress, Air Flotation, Alternating Pressure 1Bariatric Bed 1Bed, Flotation Therapy, Powered 1

Market	Identifier	Name	Class / date
UK	17593	K-0 ELITE	Class I
SA	ME0000012318SFDAA00001	Alternating Pressure MicroAir 50	—
SA	ME0000012318SFDAA00002	Alternating Pressure MicroAir 55	—

Kap Medical Corporation

Registrations by market

How these numbers were verified

Regulatory identity

Company information

FDA listed device types

Registration details (sample)

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