Facility

MEDOS INTERNATIONAL SARL

2 recall(s) on record — most severe on record: Class I.

Key facts

2recalls · worst Class I

—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)	3008114965
Establishment type	Develop Specifications But Do Not Manufacture At This Facility
Location	Chemin-Blanc 38 Le Locle Neuchatel, CH 2400
Registration status	Active · expires 2026
Parent company	Medos International SARL (owner-operator 10031083)
Brand names	CONCORDE LIFT

Activity by year

Recalls (2)

Devices registered here (1)

Intervertebral Fusion Device With Bone Graft, Lumbar
Product code MAX (opens in a new tab) · Class II · Orthopedic · 21 CFR 888.3080

Recalls & enforcement

Class IIOngoing2026-07-23
Software issue within robotic controller which may cause unintended movement of the robotic arm during bone preparation or instrument positioning.
Class IOngoing2024-02-02
Medos has received an increase in complaints for CEREBASE DA Guide Sheath with reports of fractures at the distal end, which may result in surgical procedural delay, vascular injury and in extreme rare occasions it may result in embolism.

All facilities operated by Medos International SARL

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. “MEDOS INTERNATIONAL SARL (FEI 3008114965) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3008114965-medos-international-sarl/

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