BIOSERVO AB

FDA Device Registration & Listing · Kista Stockholm, SE · Registration 3027241828

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3027241828
FEI Number
3027241828
Entity Name
BIOSERVO AB
City/State/Country
Kista Stockholm, SE
Establishment Address
Torshamnsgatan 35, Kista Stockholm 16440, SE
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device
Owner / Operator
Bioservo AB (Owner Number: 10087850)
Owner / Operator Contact Address
Torshamnsgatan 35, Kista, SE-AB 16440, SE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Carbonhand

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IQZ Hand, External Limb Component, Powered Physical Medicine Class 1 890.3420 2023-04-20

Official Correspondent

Petter Backgren

US Agent Details

Catherine Rowe Business: Greenleaf Health, Inc. Email: crowe@eliquent.com Phone: (804) 9381858

Related Public Records

Same Entity

Bioservo AB
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3027241828. Last updated year: 2026. Please use registration number 3027241828 when referencing this establishment in official correspondence.
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