BONESETTER HOLDINGS, LLC

FDA Device Registration & Listing · Plymouth, MI, US · Registration 3016472588

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
3016472588
FEI Number
3016472588
Entity Name
BONESETTER HOLDINGS, LLC
City/State/Country
Plymouth, MI, US
Establishment Address
44099 Plymouth Oaks Blvd, Suite 109, Plymouth, MI 48170, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Bonesetter Holdings, LLC (Owner Number: 10062492)
Owner / Operator Contact Address
44099 Plymouth Oaks Blvd, Suite 109, Plymouth, MI 48170, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

ABC Cement Dispenser

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OAR Injector, Vertebroplasty (Does Not Contain Cement) Orthopedic Class 1 888.4200 2020-02-03

Official Correspondent

Ronald Zimmermann

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Bonesetter Holdings, LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3016472588. Last updated year: 2026. Please use registration number 3016472588 when referencing this establishment in official correspondence.
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