Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1058002

FEI Number

1000222013

Entity Name

Technicuff Corp.

City/State/Country

LEESBURG, FL, US

Establishment Address

2525 Industrial St., LEESBURG, FL 34748, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

TECHNICUFF CORP. (Owner Number: 9010195)

Owner / Operator Contact Address

2525 INDUSTRIAL ST., --, Leesburg, FL 34748, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K942259

PMA Number

N/A

All Registered Proprietary Names

Technicuff Blood Pressure Cuff

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
DXQ	Blood Pressure Cuff	Cardiovascular	Class 2	870.1120	2008-01-02

Official Correspondent

Caroline Van Dyken

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

TECHNICUFF CORP.

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

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1058002. Last updated year: 2026. Please use registration number 1058002 when referencing this establishment in official correspondence.