EXOCAD AMERICA, INC.

FDA Device Registration & Listing · Wakefield, MA, US · Registration 3013718526

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
3013718526
FEI Number
3013718526
Entity Name
EXOCAD AMERICA, INC.
City/State/Country
Wakefield, MA, US
Establishment Address
301 Edgewater Pl Ste 330, Wakefield, MA 01880, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198
Owner / Operator
exocad GmbH (Owner Number: 10055196)
Owner / Operator Contact Address
Rosa-Parks-Str. 2, Darmstadt, DE-HE 64295, DE
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

AbutmentCAD Implant Module Ceramill Mind M-Plant PlanCAD Premium AbutmentCAD DentalDB

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PNP Dental Abutment Design Software For Dental Laboratory Dental Class 2 872.3630 2021-10-15
OUG Medical Device Data System General Hospital Class 1 880.6310 2017-06-19

Official Correspondent

Stefan Walter

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

exocad GmbH
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3011521456 EXOCAD GMBH Darmstadt Hesse, DE

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013718526. Last updated year: 2026. Please use registration number 3013718526 when referencing this establishment in official correspondence.
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