OSTEOGENE TECH CORP

FDA Device Registration & Listing · Norwood, NJ, US · Registration 3021912300

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
3021912300
FEI Number
3021912300
Entity Name
OSTEOGENE TECH CORP
City/State/Country
Norwood, NJ, US
Establishment Address
75 Oak Street, Norwood, NJ 07648, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Osteogene Tech Inc. (Owner Number: 10084587)
Owner / Operator Contact Address
75 Oak Street, Norwood, NJ 07648, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K202675
PMA Number
N/A

All Registered Proprietary Names

InRoad Synthetic Bone Graft

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LYC Bone Grafting Material, Synthetic Dental Class 2 872.3930 2022-03-09

Official Correspondent

James OConnor

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Osteogene Tech Inc.
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
K052493 Steiner Laboratories SOCKET GRAFT 2006-06-09

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3021912300. Last updated year: 2026. Please use registration number 3021912300 when referencing this establishment in official correspondence.
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