Facility

EXOCAD GMBH

1 recall(s) on record — most severe on record: Class II.

Key facts

1recalls · worst Class II

—inspections in our data

—warning letters in our data

Recalls are listed for the parent company: openFDA recall records do not name a facility. How we attribute records

FDA Establishment Identifier (FEI)	3011521456
Establishment type	Manufacture Medical Device
Location	Rosa-Parks-Str. 2 Darmstadt Hesse, DE 64295
Registration status	Active · expires 2026
Parent company	exocad GmbH (owner-operator 10055196)
Brand names	Implant Module; AbutmentCAD; Ceramill Mind M-Plant; PlanCAD Premium AbutmentCAD

Activity by year

Recalls (1)

Devices registered here (1)

Dental Abutment Design Software For Dental Laboratory
Product code PNP (opens in a new tab) · Class II · Dental · 21 CFR 872.3630

Recalls & enforcement

Class IIOngoing2023-08-17
A software library filtering error has been discovered which occurs when users are using the Step-by-Step Full Drill Protocol export functionality of exoplan 3.1 Rijeka. When a guided surgery treatment approach is selected, along with a Step-by-Step Full Drill Protocol export imp…

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “EXOCAD GMBH (FEI 3011521456) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3011521456-exocad-gmbh/

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