Facility

SICAT GMBH & CO. KG

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)	3006098230
Establishment type	Export Device to the United States But Perform No Other Operation on Device
Location	Friesdorfer Strasse 131-135 BONN North Rhine-Westphalia, DE 53175
Registration status	Active · expires 2026
Parent company	SICAT GMBH & CO. KG (owner-operator 9087842)
Brand names	Endo Dental Bur

Activity by year

Recalls (1)

Devices registered here (1)

Drill, Dental, Intraoral
Product code DZA (opens in a new tab) · Class I · Dental · 21 CFR 872.4130

Recalls & enforcement

Class IITerminated2020-07-15
A dentist found implant positions are not correctly exported from the implant planning software SICAT IMPLANT V2.0 - for the specific export format CMG.DXD.

All facilities operated by SICAT GMBH & CO. KG

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. “SICAT GMBH & CO. KG (FEI 3006098230) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3006098230-sicat-gmbh-co-kg/

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