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NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.

USA · Canoga Park

✓ Record-verifiedregistrations found in 3 markets

This company has registrations in United States, Brazil, Canada — 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

46listed device types

Class I 31Class II 15Class III 0

plus 46 registration records and 8 510(k)

UKUnited KingdomMHRA PARD

pendingnot queried

BRBrazilANVISA

1registered devices

Class II 1

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

SASaudi ArabiaSFDA

0registered imported devices

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

CACanadaMDALL

0active device licences

6 including historic records

TWTaiwanTFDA

0valid device licences

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 States46 registration records, 8 510(k), 0 PMA, 63 excluded

Brazil1 confirmed, 33 excluded

Saudi Arabia0 confirmed, 5 excluded

Canada0 confirmed, 7 excluded

Manufacturer names merged into this page: NATIONAL ADVANCED ENDOSCOPY DEVICES, INC. · NATIONAL ADVANCED ENDOSCOPY DEVICES INC. · National Advanced Endoscopy Devices Inc

FDA 510(k) clearances by year

31999 · K993689

22008 · K081553

12010 · K102663

12015 · K141515

12017 · K170285

FDA listed device types

showing 8 of 46

Motor, Surgical Instrument, Ac-Powered 1Punch, Nasal 1Instrument, Ligature Passing And Knot Tying 1Camera, Television, Endoscopic, Without Audio 1Clamp 1Cannula, Sinus 1Knife, Nasal 1Gouge, Nasal, Ent 1

Market	Identifier	Name	Class / date
US	K170285	AED Sinuscope	2017-08-01
US	K141515	AED HYSTEROSCOPE AND ACCESSORIES	2015-01-07
US	K102663	AED RESECTOSCOPE	2010-12-30
BR	80369740001	AED ENDOVIEW	Class II

NATIONAL ADVANCED ENDOSCOPY DEVICES, INC.

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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