BRISAR INDUSTRIES INC

FDA Device Registration & Listing · Paterson, NJ, US · Registration 3003559457

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3003559457
FEI Number
3003559457
Entity Name
BRISAR INDUSTRIES INC
City/State/Country
Paterson, NJ, US
Establishment Address
76 Wood Street, Paterson, NJ 07524, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
BRISAR/DELVCO PACKAGING SERVICES (Owner Number: 9071034)
Owner / Operator Contact Address
150 EAST 7TH ST., --, Paterson, NJ 07524, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

4K Score Specimen Collection Kit VIV for Your V Hero Patch + Hydrate Kit Hero Ultimate Patch Pack Hero Patch Icon Kit Might Patch Duo Dura Derm Sport POPS Post Operative Plus Exofin Mastic Hero Ultimate Patch Pack Hero Patch + Hydrate Kit Hero Patch Icon Kit Might Patch Duo

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QRF Multi-Analyte Test System With Algorithmic Analysis For Detection Of Prostate Cancer Unknown Class 3 N/A 2023-11-13
EFW Toothbrush, Manual Dental Class 1 872.6855 2018-12-21
HEB Tampon, Menstrual, Unscented Obstetrics/Gynecology Class 2 884.5470 2021-12-28
NAD Dressing, Wound, Occlusive General, Plastic Surgery Class 1 878.4020 2023-11-13
KMF Bandage, Liquid General Hospital Class 1 880.5090 2020-12-28
KGX Tape And Bandage, Adhesive General Hospital Class 1 880.5240 2018-12-21
NAC Dressing, Wound, Hydrophilic General, Plastic Surgery Class 1 878.4018 2025-08-04

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

BRISAR/DELVCO PACKAGING SERVICES
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
K973236 Procter & Gamble Co. CREST TOOTHBRUSH WITH MICROSHIELD 1998-03-11
K923985 Personal Products Co. UNSCENTED MENSTRUAL TAMPON 1993-02-19
K151170 Tosama, D.O.O. Tosama 100% Organic Cotton Menstrual Tampon 2015-07-02
K930149 Kimberly-Clark Corp. KOTEX DISCRETE DIGITAL TAMPONS, REG.,SUPER,SUPER+ 1994-03-02
K881936 Iberhospitex, S.A. OPER-FILM-ADHESIVE MEMBRANE 1988-08-31

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0013-2019 COVIDIEN LLC 1
Kerlix AMD Antimicrobial Bandage Roll, 6 Ply, 4-1/2 x 12.3 (11.4 cm x 3.7m), REF 3332 Product Usage- as both primary and secondary dressing containing PHMB (polyhexamethylene biguanide) to resist bacterial colonization within the dressing and bacterial penetration through the dressing.
Z-0014-2019 COVIDIEN LLC 1
Kerlix Bandage Roll, 100% Cotton, 6 Ply, Large 4-1/2 x 4-1/8 yd (11.4 cm x 3.7m), REF 6715 Product Usage: Used as both primary and secondary dressing for bandaging heads, limbs and difficult-to-dress wounds.
Z-0015-2019 COVIDIEN LLC 1
Kerlix Gauze Roll, 6 Ply, Large 4-1/2 x 4-1/8 yd (11.4 cm x 3.7m) Stretched, REF 7880 Product Usage: Used as both primary and secondary dressing for bandaging heads, limbs and difficult-to-dress wounds.
Z-0016-2019 COVIDIEN LLC 1
Kerlix Bandage Roll, 100 Cotton, 8 Ply, Large 4-1/2 x 9.3 (11.4 cm x 2.8 m), REF 6716 Product Usage: Used as both primary and secondary dressing for bandaging heads, limbs and difficult-to-dress wounds.
Z-0017-2019 COVIDIEN LLC 1
Dermacea Gauze Fluff Roll, 6 Ply, 4-1/2 x 4-1/8 yd (11.4 cm x 3.7 m), REF 441103 Product Usage: Used as both primary and secondary dressing for bandaging heads, limbs and difficult-to-dress wounds.

Similar Registrations

Registration Number Establishment Name Location
3003652672 BioReference Health, LLC Elmwood Park, NJ, US
3011015335 CLEVELAND DIAGNOSTICS, INC. Cleveland, OH, US
3006149964 POWERLINK CREATIONS (ZHONGSHAN) CORPORATION Zhongshan Guangdong, CN
3002762071 EBNAT AG Ebnat-Kappel Sankt Gallen, CH
3026482909 WALDKRAFT GMBH Todtnau Baden-Wurttemberg, DE
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003559457. Last updated year: 2026. Please use registration number 3003559457 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.