Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

9615414

FEI Number

3003769089

Entity Name

GLUSTITCH, INC.

City/State/Country

Delta British Columbia, CA

Establishment Address

No. 307 7188 PROGRESS WAY, Delta British Columbia V4G 1M6, CA

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

GLUSTITCH, INC. (Owner Number: 9035904)

Owner / Operator Contact Address

#307 7188 PROGRESS WAY, --, Delta, CA-BC V4G 1M6, CA

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K071484

PMA Number

N/A

All Registered Proprietary Names

GluSeal®90 GLUSEAL(ST) GluSeal®90 GLUSEAL0.5(ST) GluSeal®90 GLUSEAL(ST)(C) GluSeal® GLUSEAL5V GluSeal® GLUSEAL(C) GluSeal® GLUSEAL5C GluSeal® GLUSEAL(V) GluSeal® GLUSEAL5(C)HV PeriAcryl®90 P-ACRYL2(V) PeriAcryl®90 P-ACRYLU(V)HV PeriAcryl®90 P-ACRYL9(V)HV PeriAcryl®90 P-ACRYLU(V) PeriAcryl®90 P-ACRYL5(V)HV PeriAcryl®90 P-ACRYLU(C) PeriAcryl®90 P-ACRYL2(C) PeriAcryl®90 P-ACRYL5(V) PeriAcryl®90 P-ACRYL5(C) PeriAcryl®90 P-ACRYL9(V)

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KMF	Bandage, Liquid	General Hospital	Class 1	880.5090	2012-10-22
KMF	Bandage, Liquid	General Hospital	Class 1	880.5090	2007-12-03
EMA	Cement, Dental	Dental	Class 2	872.3275	2012-10-22

Official Correspondent

DON BLACKLOCK

US Agent Details

Arthur S. Goddard Email: asjgoddard@aol.com Phone: (216) 2335722

Related Public Records

Same Entity

GLUSTITCH, INC.

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
K972485	Arent, Fox, Kintner, Plotkin & Kahn	CIMPAT N	1997-09-08
K982895	Sterngold/Implamed	STERNOMEGA COMPOMER CEMENT	1998-10-09
K033068	Voco GmbH	IONOFIL COLOR AC	2003-10-31
K062064	Southern Dental Industries, Inc.	RIVA BOND LC	2006-11-09
K940030	Bisco, Inc.	BISCO COMPOSITE	1994-02-04

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 9615414. Last updated year: 2026. Please use registration number 9615414 when referencing this establishment in official correspondence.