Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008821638

FEI Number

3008821638

Entity Name

ABSORBEST AB

City/State/Country

Kisa Ostergotland, SE

Establishment Address

Klintvagen 1, Kisa Ostergotland 59039, SE

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device

Owner / Operator

Absorbest AB (Owner Number: 10034338)

Owner / Operator Contact Address

Klintvagen 1, Kisa, SE-E 59039, SE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

DryMax FOAM DryMax GENTLE DryMax SOFT DryMax BORDER Absorbest Super Foam

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NAC	Dressing, Wound, Hydrophilic	General, Plastic Surgery	Class 1	878.4018	2010-11-24

Official Correspondent

Ulrika Malmen

US Agent Details

Yong Sun Business: Emergo Global Representation LLC Email: USAgent@ul.com Phone: (512) 3279997

Related Public Records

Same Entity

Absorbest AB

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

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008821638. Last updated year: 2026. Please use registration number 3008821638 when referencing this establishment in official correspondence.