Facility

BEMER Int. AG

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)	3009102830
Establishment type	Export Device to the United States But Perform No Other Operation on Device; Manufacture Medical Device
Location	Austrasse 15 Triesen, LI 9495
Registration status	Active · expires 2026
Parent company	BEMER Int. AG (owner-operator 10035841)
Brand names	BEMER Therapy System Evo, B.Box Evo, B.Body Evo, B.Bed Evo, B.Sit Evo, B.Pad Evo, B.Spot Evo

Activity by year

Recalls (1)

Devices registered here (1)

Stimulator, Muscle, Powered, For Muscle Conditioning
Product code NGX (opens in a new tab) · Class II · Physical Medicine · 21 CFR 890.5850

Recalls & enforcement

Class IITerminated2021-01-13
There potential that electromagnetic fields generated in the therapy system may cause technical defects in a patient using an insulin pumps or a malfunction of a pacemaker.

All facilities operated by BEMER Int. AG

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. “BEMER Int. AG (FEI 3009102830) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3009102830-bemer-int-ag/

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