Home›USA›AUTOMATED MEDICAL PRODUCTS CORP.

AUTOMATED MEDICAL PRODUCTS CORP.

USA · Sewaren

✓ Record-verifiedregistrations found in 4 markets

This company has registrations in United States, Brazil, Taiwan, Australia — 4 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

5listed device types

Class I 5Class II 0Class III 0

plus 5 registration records and 6 510(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

TWTaiwanTFDA

1valid device licences

Class I 1

SGSingaporeHSA SMDR

pendingnot queried

KRSouth KoreaMFDS GMP

pendingnot queried

AUAustraliaTGA ARTG

1active ARTG entries

Class I 1

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 States5 registration records, 6 510(k), 0 PMA, 7 excluded

Brazil1 confirmed, 0 excluded

Canada0 confirmed, 1 excluded

Manufacturer names merged into this page: AUTOMATED MEDICAL PRODUCTS CORP.

FDA 510(k) clearances by year

11979 · K792145

11983 · K832827

31994 · K942818

11995 · K942910

FDA listed device types

Retractor 1Instrument, Manual, Surgical, General Use 1Tray, Surgical, Instrument 1Retractor, Vaginal 1Hook, Gastro-Urology 1

Market	Identifier	Name	Class / date
US	K942910	DEEPVISON	1995-07-21
US	K942818	DEEP SUTURE	1994-08-25
US	K942002	RETRACTOR	1994-05-17
BR	81747159020	SISTEMA DE RETRAÇÃO IRON INTERN	Class II

AUTOMATED MEDICAL PRODUCTS CORP.

Registrations by market

How these numbers were verified

Company information

FDA 510(k) clearances by year

FDA listed device types

Registration details (sample)

Similar companies