BO&BO LTD

FDA Device Registration & Listing · Amir Northern, IL · Registration 3043587013

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
3043587013
FEI Number
3043587013
Entity Name
BO&BO LTD
City/State/Country
Amir Northern, IL
Establishment Address
1 Bait Rishon Bamoledet, Amir Northern 121400, IL
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Bo&Bo Ltd (Owner Number: 10095174)
Owner / Operator Contact Address
1 Bait Rishon Bamoledet, Amir, IL-Z 121400, IL
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

BoBo Motion 2 BoBo Pro 2 BoBo Wobbly BoBo Home BoBo Dice BoBo Dice Pro

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LBB Dynamometer, Ac-Powered Orthopedic Class 2 888.1240 2026-02-03
PKS Exerciser, Non-Measuring For Stroke Rehabilitation Physical Medicine Class 1 890.5370 2026-02-03
JFA Exerciser, Finger, Powered Physical Medicine Class 1 890.5410 2026-02-03

Official Correspondent

Gadi Nir

US Agent Details

Gadi Nir Business: BOBO USA INC Email: gadi@bobo-balance.com Phone: (888) 3003153

Related Public Records

Same Entity

Bo&Bo Ltd
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 3043587013. Last updated year: 2026. Please use registration number 3043587013 when referencing this establishment in official correspondence.
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