CLEMDE S.A. DE C.V.

FDA Device Registration & Listing · MEXICO, DF Ciudad de Mexico, MX · Registration 3008494285

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
3008494285
FEI Number
3008494285
Entity Name
CLEMDE S.A. DE C.V.
City/State/Country
MEXICO, DF Ciudad de Mexico, MX
Establishment Address
AV. LA FORTUNA No.136 COL INDUSRRIAL C.P, C.P., MEXICO, DF Ciudad de Mexico 07800, MX
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
CLEMDE S.A. DE C.V. (Owner Number: 10033284)
Owner / Operator Contact Address
AV LA FORTUNA 136, COL INDUSTRIAL, MEXICO CITY, MX-NOTA 07800, MX
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

PF Keep / Cad Cam Peek Block Partial Flex

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EBI Resin, Denture, Relining, Repairing, Rebasing Dental Class 2 872.3760 2024-02-27
EBF Material, Tooth Shade, Resin Dental Class 2 872.3690 2024-02-27
EBG Crown And Bridge, Temporary, Resin Dental Class 2 872.3770 2024-02-27
EKO Denture Preformed (Partially Prefabricated Denture) Dental Class 2 872.3600 2016-12-09

Official Correspondent

Francisco Cabrera

US Agent Details

Mariana Correa Email: apcoconsultores@gmail.com Phone: (956) 4141294

Related Public Records

Same Entity

CLEMDE S.A. DE C.V.
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
K800400 Dentsply Intl. MAXUM DENTURE RESIN 1980-03-12
K033020 Cmp Industries, LLC IMPAK ACRYLIC REPAIR RESIN LIQUID 2003-12-19
K952662 Jeneric/Pentron, Inc. COMP=FLOW 1995-08-28
K171147 Bisco, Inc. REVEAL Bulk 2017-08-04
K770922 Espe GmbH (Us) DENTAL RESTORATIVE IN CAPSULES 1977-06-01

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0028-2020 Voco GmbH Anton-Flettner-Str. 1-3 Cuxhaven Germany 2
Grandio SO Heavy Flow Caps, Color A3 - Product Usage: Filling minimally invasive cavities of all classes - Filling small class I cavities and extended fissure sealing - Filling class II - V cavities including V-shaped defects and cervical caries - Blocking out undercuts - Lining or coating cavities - Repairing fillings and veneers - Luting translucent prosthetic pieces (e.g., full ceramic crowns, etc.).

Similar Registrations

Registration Number Establishment Name Location
3017374693 STRATASYS LTD - Headquarter Rehovot Central, IL
2950685 CO-ORAL-ITE DENTAL MFG. CO. DIAMOND SPRINGS, CA, US
3032727 TALON ACRYLICS, INC. Winchester, OR, US
3008320092 Shandong Huge Dental Material Corporation Rizhao Shandong, CN
1410097 GC AMERICA INC. ALSIP, IL, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008494285. Last updated year: 2026. Please use registration number 3008494285 when referencing this establishment in official correspondence.
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