Facility

WISSNER-BOSSERHOFF GMBH

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

Key facts

1recalls · worst Class II

1inspections · worst OAI

1warning letters

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

FDA Establishment Identifier (FEI)	3015979371
Establishment type	Manufacture Medical Device
Location	Hauptstrasse 4-6 Wickede (Ruhr) North Rhine-Westphalia, DE 58739
Registration status	Active · expires 2026
Parent company	wissner-bosserhoff GmbH (owner-operator 10061587)
Brand names	sentida 6 USA; sentida 03; sentida 6; sentida 7-i; sentida 7-i wohnlich USA; sentida 1; sentida 5; sentida sc-xl USA; sentida sc USA; sentida sc-xxl USA; sentida 5-xxl

Activity by year

Recalls (1)
Inspections (1)
Warning letters (1)

Devices registered here (1)

Bed, Therapeutic, Ac-Powered, Adjustable Home-Use
Product code LLI (opens in a new tab) · Class II · General Hospital · 21 CFR 880.5100

Recalls & enforcement

Class IIOngoing2022-07-11
When the handset is disconnected from the power mains, and mains operation is restored, the handset is reset to the preset Resident mode. In this mode, the backrest, legrest, and height adjustment can be moved.

FDA inspections (1)

OAI2024-04-25
Official Action Indicated · Compliance: Devices; Project Evaluation: Devices; Postmarket Assurance: Devices · citations posted

Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.

FDA warning letters (1)

Warning Letter2024-08-30
Warning Letter (opens in a new tab) · Wickede (Ruhr)

Source: U.S. FDA Compliance Actions Dashboard (opens in a new tab) (device warning letters, 2016–present). Data as of 2026-10-06. Each link opens an FDA search for the letter; FDA can take several weeks to post a letter, so a very recent one may not appear yet.

All facilities operated by wissner-bosserhoff GmbH

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. “WISSNER-BOSSERHOFF GMBH (FEI 3015979371) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3015979371-wissner-bosserhoff-gmbh/

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