SOUTHERN CARBIDE SPECIALISTS, INC.

FDA Device Registration & Listing · Quitman, GA, US · Registration 3008609789

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
3008609789
FEI Number
3008609789
Entity Name
SOUTHERN CARBIDE SPECIALISTS, INC.
City/State/Country
Quitman, GA, US
Establishment Address
901 N Highland Rd, Quitman, GA 31643, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Southern Carbide Specialists, Inc. (Owner Number: 10042627)
Owner / Operator Contact Address
901 N. Highland St., Quitman, GA 31643, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HTT Burr, Orthopedic Orthopedic Class 1 888.4540 2012-12-14

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Southern Carbide Specialists, Inc.
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 3008609789. Last updated year: 2026. Please use registration number 3008609789 when referencing this establishment in official correspondence.
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