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Verathon Incorporated

USA · Bothell

✓ Record-verifiedregistrations found in 8 markets

This company has registrations in United States, Saudi Arabia, Canada, Taiwan, Singapore, Australia, Hong Kong, Israel — 8 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

6listed device types

Class I 2Class II 4Class III 0

plus 10 registration records and 5 510(k)

UKUnited KingdomMHRA PARD

pendingnot queried

BRBrazilANVISA

0registered devices

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

SASaudi ArabiaSFDA

1registered imported devices

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

CACanadaMDALL

8active device licences

Class II 2Class III 6

19 including historic records

TWTaiwanTFDA

1valid device licences

Class II 1

SGSingaporeHSA SMDR

5device registrations

CLASS B 5

KRSouth KoreaMFDS GMP

pendingnot queried

AUAustraliaTGA ARTG

3active ARTG entries

Class I 2IIa 1

HKHong KongMDACS

2valid listings

Class II 2

ILIsraelAMAR

2registrations

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 States10 registration records, 5 510(k), 0 PMA, 3 excluded

Saudi Arabia1 confirmed, 3 excluded

Canada8 confirmed, 1 excluded

Manufacturer names merged into this page: Verathon Inc. · VERATHON INC.

FDA 510(k) clearances by year

12007 · K071217

12008 · K082456

12009 · K090214

12015 · K153101

12017 · K172356

FDA listed device types

Bronchoscope (Flexible Or Rigid) 1Uroflowmeter 1Transducer, Ultrasonic, Diagnostic 1System, Imaging, Pulsed Echo, Ultrasonic 1Stylet, Tracheal Tube 1Laryngoscope, Rigid 1

Registration details (sample)

Market	Identifier	Name	Class / date
US	K172356	BladderScan Prime PLUS System	2017-09-15
US	K153101	BladderScan Prime System	2015-11-19
US	K090214	VERATHON INC. BLADDERSCAN BVM 9500 ULTRASOUND	2009-03-13
SA	ME0000007388SFDAA00002	GlideScope® Ranger GVL	—
CA	30417	BLADDERSCAN BVI 5000: NONINVASIVE BLADDER VOLUME INSTRUMENT	Class III
CA	30418	BLADDERMANAGER PCI5000: PERSONAL CARE INSTRUMENT	Class III
CA	63380	BLADDERMASS BVM 6500	Class III

Verathon Incorporated

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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