Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3042752784

FEI Number

3042752784

Entity Name

SINBON-OHIO

City/State/Country

Englewood, OH, US

Establishment Address

1 Sinbon Way, Englewood, OH 45315, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

SINBON-Ohio (Owner Number: 10094680)

Owner / Operator Contact Address

1 Sinbon Way, Englewood, OH 45315, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
SEC	Wearable Fall Injury Prevention Device	Physical Medicine	Class 2	890.3780	2025-12-16

Official Correspondent

Kenneth Kocks

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

SINBON-Ohio

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

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3042752784. Last updated year: 2026. Please use registration number 3042752784 when referencing this establishment in official correspondence.