CAMP SCANDINAVIA AB

FDA Device Registration & Listing · HELSINGBORG Skane, SE · Registration 8030901

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
8030901
FEI Number
3005150907
Entity Name
CAMP SCANDINAVIA AB
City/State/Country
HELSINGBORG Skane, SE
Establishment Address
38 KARBINGATAN, HELSINGBORG Skane SE-254 67, SE
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device
Owner / Operator
Allard Support for Better Life AB (Owner Number: 8030901)
Owner / Operator Contact Address
38 KARBINGATAN, --, HELSINGBORG, SE-NOTA SE-254 67, SE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

VISSION CSUS FORGE M2 Aosuo prosthetic foot shell Vission S.O.T AND COMPONENTS SELECTION WRIST SPLINTS COMBO MultiMotion Combo

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IQJ Splint, Clavicle Physical Medicine Class 1 890.3490 2010-07-30
IPM Cover, Limb Physical Medicine Class 1 890.3025 2024-10-10
ILH Splint, Hand, And Components Physical Medicine Class 1 890.3475 2005-07-28
ITQ Joint, Knee, External Brace Physical Medicine Class 1 890.3475 2005-07-28

Official Correspondent

No official correspondent registered.

US Agent Details

Maria Overton Business: ALLARD USA INC Email: maria.overton@allardusa.com Phone: (973) 9836000

Related Public Records

Same Entity

Allard Support for Better Life AB
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Other Registrations for Same Entity

Registration Number Establishment Name Location
3005282622 ALLARD USA INC. ROCKAWAY, NJ, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 8030901. Last updated year: 2026. Please use registration number 8030901 when referencing this establishment in official correspondence.
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