Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3006142326

FEI Number

3006142326

Entity Name

AKRUS GmbH & Co. KG

City/State/Country

Elmshorn Schleswig-Holstein, DE

Establishment Address

Otto-Hahn-Str. 3, Elmshorn Schleswig-Holstein 25337, DE

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

AKRUS GmbH & Co KG (Owner Number: 10046166)

Owner / Operator Contact Address

Otto-Hahn-Str. 3, Elmshorn, DE-SH 25337, DE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Additive Back support MBS Additive Back support (viscoel.) MBS Adapter footrest MBS ak 5010 MBS AK 150 DL IT 1060.i Sliding keyboard shelf Instrument delivery table ak 106 AK 150 DL/ST IT 760.i Footrest extension Patient Support System LSCneo Doctor stool ak 445 Doctor stool ak 446 Doctor stool ak 447

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LGX	Table, Examination, Medical, Powered	General, Plastic Surgery	Class 1	878.4960	2025-11-26
HRJ	Table, Instrument, Powered, Ophthalmic	Ophthalmic	Class 1	886.4855	2018-10-21
FQO	Table, Operating-Room, Ac-Powered	General, Plastic Surgery	Class 1	878.4960	2023-11-13
FZM	Stool, Operating-Room	General, Plastic Surgery	Class 1	878.4950	2023-04-20

Official Correspondent

No official correspondent registered.

US Agent Details

Angelika Scherp Business: Business Support International Email: info@bsi-fda.com Phone: (212) 3318358

Related Public Records

Same Entity

AKRUS GmbH & Co KG

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0036-2024	Getinge Usa Sales Inc	1	Meera Mobile Operating Table-to support and position the patient immediately before, during and after surgical interventions as well as for examination and treatment. Model Number: 7200.01F2

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006142326. Last updated year: 2026. Please use registration number 3006142326 when referencing this establishment in official correspondence.