SIGMAGRAFT, INC.

FDA Device Registration & Listing · Fullerton, CA, US · Registration 3009598981

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
3009598981
FEI Number
3009598981
Entity Name
SIGMAGRAFT, INC.
City/State/Country
Fullerton, CA, US
Establishment Address
575 Sally Pl, Fullerton, CA 92831, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
SigmaGraft, Inc. (Owner Number: 10040723)
Owner / Operator Contact Address
575 Sally Place, Fullerton, CA 92831, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
K151209
PMA Number
N/A

All Registered Proprietary Names

InterOss Maxxeus Dental Xenograft Particulates Mega-Oss BovineTM Maxxeus

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NPM Bone Grafting Material, Animal Source Dental Class 2 872.3930 2015-11-16

Official Correspondent

Elcin Chang

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

SigmaGraft, Inc.
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 3009598981. Last updated year: 2026. Please use registration number 3009598981 when referencing this establishment in official correspondence.
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