Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1416891

FEI Number

1416891

Entity Name

ANCHOR PRODUCTS CO.

City/State/Country

ADDISON, IL, US

Establishment Address

52 OFFICIAL RD., ADDISON, IL 60101, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

ANCHOR PRODUCTS CO. (Owner Number: 1416891)

Owner / Operator Contact Address

52 OFFICIAL RD., --, Addison, IL 60101, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Anchor Brand Anchor Brand Anchor Brand TISSUE RETRIEVAL SYSTEM COUNT-TAINER Anchor Brand Anchor Brand

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
JYP	Knife, Myringotomy	Ear, Nose, Throat	Class 1	874.4420	1990-11-15
GAB	Needle, Suturing, Disposable	General, Plastic Surgery	Class 1	878.4800	1990-11-15
HNN	Knife, Ophthalmic	Ophthalmic	Class 1	886.4350	1990-11-15
GCJ	Laparoscope, General & Plastic Surgery	Gastroenterology, Urology	Class 2	876.1500	2011-12-13
MMK	Container, Sharps	General Hospital	Class 2	880.5570	2008-04-22
GDL	Needle, Suturing, Reusable	General, Plastic Surgery	Class 1	878.4800	1990-11-15
HNM	Needle, Ophthalmic Suturing	Ophthalmic	Class 1	886.4350	1990-11-15

Official Correspondent

ROBERT THRUN

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ANCHOR PRODUCTS CO.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K874057	Myocure, Inc.	OPHTHALMIC TIP & BLADE SCALPELS	1987-12-23
K914997	Conmedcorp	ASP-IRRATOR	1992-01-07
K153773	Olympus Medical Systems Corp.	Disposal Lens Cleaning Sheath	2016-11-22
K940141	Micro-Medical Devices, Inc.	LAPARAOSCOPES ELECTRONIC WITH STERILE SHEATH	1994-05-19
K933812	Advanced Surgical, Inc.	ADVANCED SURGICAL, INC. CANNULA CLEANING DEVICE AND ACCESSORIES	1993-12-13

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0026-04	Surgical Specialties Corp	1	Sharpoint 2.75 mm x 3.75 mm ClearTrap Trapezoid Knife Clear Corneal Implant Angled. The product can be sold as an individual unit or in a box of 6 knives.
Z-1922-2024	Alcon Research LLC Aspex Facility	1	20 Gauge V-Lance Knife Model/Catalog Number: 8065912001 Software Version: N/A Product Description: Ophthalmic knife Component: N/A
Z-1923-2024	Alcon Research LLC Aspex Facility	1	ClearCut Sideport Knife Dual Bevel 1.2mm Angled Model/Catalog Number: 8065921541 Software Version: N/A Product Description: Ophthalmic Knife Component: N/A
Z-1924-2024	Alcon Research LLC Aspex Facility	1	ClearCut S Safety Sideport Knife 1.0mm Dual Bevel Model/Catalog Number: 8065771540 Software Version: N/A Product Description: Ophthalmic Knife Component: N/A
Z-1925-2024	Alcon Research LLC Aspex Facility	1	ClearCut S Safety Sideport Knife 1.2mm Dual Bevel Model/Catalog Number: 8065771541 Software Version: N/A Product Description: Ophthalmic Knife Component: N/A

Similar Registrations

Registration Number	Establishment Name	Location
3006098219	ADEPT MEDICAL LTD	AUCKLAND, NZ
9611283	DIMEDA INSTRUMENTE GMBH	TUTTLINGEN Baden-Wurttemberg, DE
3008719017	SUMMIT MEDICAL LLC	Saint Paul, MN, US
8040278	Falcon Surgical Co. (Pvt.) Ltd.	Sialkot Punjab, PK
3011137372	Teleflex Medical LLC	Morrisville, NC, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1416891. Last updated year: 2026. Please use registration number 1416891 when referencing this establishment in official correspondence.