SPFM, L.P.

FDA Device Registration & Listing · San Antonio, TX, US · Registration 3009506228

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
3009506228
FEI Number
3004266672
Entity Name
SPFM, L.P.
City/State/Country
San Antonio, TX, US
Establishment Address
4310 West Ave, San Antonio, TX 78213, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Ritter Implants GmbH and Co. KG (Owner Number: 10039754)
Owner / Operator Contact Address
4310 West Ave., San Antonio, TX 78213, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K231513
PMA Number
N/A

All Registered Proprietary Names

Oral Matrix

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NPL Barrier, Animal Source, Intraoral Dental Class 2 872.3930 2025-08-06

Official Correspondent

Olha Niziaieva

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Ritter Implants GmbH and Co. KG
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3009528809 Ritter Implants GmbH & Co. KG Biberach Baden-Wurttemberg, DE

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009506228. Last updated year: 2026. Please use registration number 3009506228 when referencing this establishment in official correspondence.
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