Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3003622639

FEI Number

3003622639

Entity Name

BARRINGTON VENTURES, LTD

City/State/Country

Barrington, IL, US

Establishment Address

28W206 COMMERCIAL AVE, Barrington, IL 60010, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

Barrington Ventures, LTD (Owner Number: 10029782)

Owner / Operator Contact Address

28W206 Commercial Avenue, Unit B, Barrington, IL 60010, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

BV Medical BV Medical BV Medical BV Medical BV Medical BV Medical KaWe BV Medical BV Medical BV Medical BV Medical

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
DXQ	Blood Pressure Cuff	Cardiovascular	Class 2	870.1120	2013-06-11
FRI	Scale, Stand-On, Patient	General Hospital	Class 1	880.2700	2017-12-15
LRW	Scissors, General, Surgical	General, Plastic Surgery	Class 1	878.4800	2018-05-15
CAF	Nebulizer (Direct Patient Interface)	Anesthesiology	Class 2	868.5630	2014-02-04
LDE	Stethoscope, Manual	Cardiovascular	Class 1	870.1875	2018-05-15
GEN	Forceps, General & Plastic Surgery	General, Plastic Surgery	Class 1	878.4800	2018-08-22
FLL	Continuous Measurement Thermometer	General Hospital	Class 2	880.2910	2017-12-15
FLL	Continuous Measurement Thermometer	General Hospital	Class 2	880.2910	2017-12-15
FXG	Specula Accessories	General, Plastic Surgery	Class 1	878.1800	2018-09-20
DXQ	Blood Pressure Cuff	Cardiovascular	Class 2	870.1120	2013-06-11
KYT	Light, Examination, Medical, Battery Powered	General Hospital	Class 1	880.6350	2018-08-03
DXQ	Blood Pressure Cuff	Cardiovascular	Class 2	870.1120	2019-05-24
DQA	Oximeter	Cardiovascular	Class 2	870.2700	2014-02-04
ERA	Otoscope	Ear, Nose, Throat	Class 1	874.4770	2017-12-15

Official Correspondent

Phillip Hoggstrom

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Barrington Ventures, LTD

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
K831001	Frontier Products	UNICUFF-BLOOD PRESSURE CUFF	1983-07-28
K253089	Shenzhen Best Electronics Co., Ltd.	NIBP Cuff (BCS-112, BCS-212, BCS-312, BCS-412, BCS-512, BCS-612, BCS-712, BCS-122, BCS-222, BCS-322, BCS-422, BCS-522, BCS-622, BCS-722, BCD-112, BCD-212, BCD-312, BCD-412, BCD-512, BCD-612, BCD-712, BCD-122, BCD-222, BCD-322, BCD-422, BCD-522, BCD-622, BCD-722)	2026-02-13
K972301	Rudolf Riester GmbH & Co. KG	BIG BEN SQUARE, BIG BEN ROUND	1997-09-17
K163485	Adherium (Nz), Ltd.	SmartTouch	2017-08-30
K781467	Travenol Laboratories, S.A.	U-FLOAT VALVE 2D9023	1978-09-07

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0020-2019	Oridion Medical 1987 Ltd. Har Hotzvim Industrial	2	CAPNOSTREAM 20 (US) N, Part Number CS08651
Z-0022-2019	Oridion Medical 1987 Ltd. Har Hotzvim Industrial	2	CAPNOSTREAM 20P (US) N - ROHS, Part Number CS08651-02
Z-0023-2019	Oridion Medical 1987 Ltd. Har Hotzvim Industrial	2	CAPNOSTREAM 20P (US) N - ROHS, Part Number CS08651-03
Z-0028-2019	Oridion Medical 1987 Ltd. Har Hotzvim Industrial	2	Capnostream20 (US) M, Part Number CS08653
Z-0029-2019	Oridion Medical 1987 Ltd. Har Hotzvim Industrial	2	Capnostream20 (US) M W/PRINTER, Part Number CS08659

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3009154535	WENZHOU KANGSHUN MEDICAL DEVICES CO.,LTD.	Wenzhou City Zhejiang, CN
1058002	Technicuff Corp.	LEESBURG, FL, US
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003622639. Last updated year: 2026. Please use registration number 3003622639 when referencing this establishment in official correspondence.