DEHEER ORTHOPEDICS

FDA Device Registration & Listing · Carmel, IN, US · Registration 3030149892

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
3030149892
FEI Number
3030149892
Entity Name
DEHEER ORTHOPEDICS
City/State/Country
Carmel, IN, US
Establishment Address
387 Ridge Point Drive, Carmel, IN 46032, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
DeHeer Orthopedics (Owner Number: 10089477)
Owner / Operator Contact Address
387 Ridge Point Drive, Carmel, IN 46032, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Baumann GRS

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MDM Instrument, Manual, Surgical, General Use General, Plastic Surgery Class 1 878.4800 2023-12-11

Official Correspondent

Alex DeHeer

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

DeHeer Orthopedics
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 3030149892. Last updated year: 2026. Please use registration number 3030149892 when referencing this establishment in official correspondence.
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