Facility

SYNTHES GMBH / Synthes Produktions 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)	3002807305
Establishment type	Manufacture Medical Device
Location	EIMATTSTRASSE 3 Oberdorf, Baselland Basel-Landschaft, CH CH-4436
Registration status	Active · expires 2026
Parent company	SYNTHES GMBH / Synthes Produktions GmbH (owner-operator 9071542)
Brand names	bone grafting material

Activity by year

Recalls (1)

Devices registered here (1)

Bone Grafting Material, Synthetic
Product code LYC (opens in a new tab) · Class II · Dental · 21 CFR 872.3930

Recalls & enforcement

Class IITerminated2020-06-16
One lot of MatrixMIDFACE Emergency Screw 1.8mm, self-tapp, L 12mm, in Clip was packaged with a body clip etched with a 3 (representing 3mm) when it should have been packaged with body clip etched with a 12 (representing 12mm).

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. “SYNTHES GMBH / Synthes Produktions GmbH (FEI 3002807305) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3002807305-synthes-gmbh-synthes-produktions-gmbh/

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