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ANCHOR PRODUCTS COMPANY INC.

USA · Addision

✓ Record-verifiedregistrations found in 2 markets

This company has registrations in United States, Canada — 2 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

9listed device types

Class I 7Class II 2Class III 0

plus 9 registration records and 7 510(k)

UKUnited KingdomMHRA PARD

pendingnot queried

BRBrazilANVISA

0registered devices

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

1active device licences

Class II 1

5 including historic records

TWTaiwanTFDA

pendingnot queried

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 States9 registration records, 7 510(k), 0 PMA, 6 excluded

Canada1 confirmed, 0 excluded

Manufacturer names merged into this page: ANCHOR PRODUCTS CO. · ANCHOR PRODUCTS COMPANY INC.

FDA 510(k) clearances by year

11979

11983

11987

11988

11998

12006

12009

FDA listed device types

showing 8 of 9

Knife, Ophthalmic 1Needle, Ophthalmic Suturing 1Needle, Suturing, Disposable 1Instrument, Surgical, Non-Powered 1Needle, Suturing, Reusable 1Needle, Tonsil Suturing 1Knife, Myringotomy 1Container, Sharps 1

Registration details (sample)

Market	Identifier	Name	Class / date
US	K091930	ANCHOR LAPAROSCOPIC TISSUE RETRIEVAL SYSTEM, MODEL TRS100SB	2009-09-23
US	K061555	ANCHOR LAPARSCOPIC TISSUE RETIEVAL SYSTEM	2006-08-31
US	K982073	ANCHOR LAPAROSCOPIC TISSUE RETRIEVAL SYSTEM	1998-09-22
CA	80737	LAPAROSCOPIC TISSUE RETRIEVAL BAG	Class II

ANCHOR PRODUCTS COMPANY 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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