Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3003595336

FEI Number

3003595336

Entity Name

TECH GROUP GRAND RAPIDS, INC.

City/State/Country

GR, MI, US

Establishment Address

3116 N. WILSON COURT NW, GR, MI 49534, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

WEST PHARMACEUTICAL SERVICES, INC. (Owner Number: 2514921)

Owner / Operator Contact Address

530 Herman O. West Drive, Exton, PA 19341, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Filter, infusion line Syringe, piston Syringe, Piston Filter, infusion line Filter, infusion line

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FPB	Filter, Infusion Line	General Hospital	Class 2	880.5440	2013-02-20
FMF	Syringe, Piston	General Hospital	Class 2	880.5860	2013-02-20
FPB	Filter, Infusion Line	General Hospital	Class 2	880.5440	2013-02-20
FPB	Filter, Infusion Line	General Hospital	Class 2	880.5440	2013-02-20

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

WEST PHARMACEUTICAL SERVICES, INC.

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

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3015176617	West Pharmaceutical Services AZ, Inc.	Scottsdale, AZ, US
3010893867	Tech Group Europe Limited t/a West	Mulhaddart Dublin, IE
3005042488	West Contract Manufacturing, LLC	Cidra, PR, US
2032861	West Pharmaceutical Services Arizona, Inc.	Tempe, AZ, US
2032862	West Pharmaceutical Services AZ, Inc.	SCOTTSDALE, AZ, US

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K880350	Honway International Co.	YUE/FA DISPOSABLE SYRINGE	1988-02-16
K003571	Terumo Medical Corp.	SERONO FOR USE WITH GONAL-F 1200IU MULTI-DOSE ONLY AT 600IU/ML SYRINGE	2001-02-12

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0003-04	Liberty Medical Supplies	2	Liberty brand Insulin Syringes for use with U-100 insulin, 1/2 cc X 30G X 5/16'' syringes
Z-0004-04	Liberty Medical Supplies	2	Liberty brand Insulin Syringes for use with U-100 insulin, 1 cc X 29G X 1/2 '' insulin syringes
Z-0005-04	Liberty Medical Supplies	2	Liberty brand Insulin Syringes for use with U-100 insulin, 1/2 cc X 29G X 1/2 '' insulin syringes
Z-0005-2024	Fresenius Medical Care Holdings, Inc.	2	10ML SYRINGE LUER LOCK W/OUT NEEDLE, Part Number 15-R010-0, 100 per box, 12 boxes to a case
Z-0006-2024	Fresenius Medical Care Holdings, Inc.	2	10ML SYRINGE LUER LOCK W/NEEDLE, Part Number 15-10ML-0, 100 per box, 12 boxes per case

Similar Registrations

Registration Number	Establishment Name	Location
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1422078	DOUGLAS MEDICAL PRODUCTS, INC	Mundelein, IL, US
1319639	Sterigenics U.S., LLC	Queensbury, NY, US
3015276780	TAM VIET DISTRIBUTION COMPANY LIMITED	HO CHI MINH, VN
3008132398	Sterigenics UK Limited	Alfreton Derbyshire, GB

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003595336. Last updated year: 2026. Please use registration number 3003595336 when referencing this establishment in official correspondence.