Absorbest AB
US Last updated 23 May 2026
- Devices
- 30
- Registries
- GUDIDEUDAMEDFDA
- FDA recalls
- 0
Catalogue
DryMax SOFT F60014/10 Ref F60014/10
Absorbest Super Foam F60046/10 Ref F60046/10
DryMax SOFT F60011/10 Ref F60011/10
DryMax FOAM F60044/10 Ref F60044/10
DryMax BORDER F50515/10 Ref F50515/10
DryMax FOAM F60045/10 Ref F60045/10
Absorbest Super Foam F60041/10 Ref F60041/10
DryMax FOAM F60043/10 Ref F60043/10
DryMax SOFT F60019/10 Ref F60019/10
DryMax SOFT F60012/10 Ref F60012/10
Absorbest Super Foam F60044/10 Ref F60044/10
Absorbest Super Foam F60043/10 Ref F60043/10
DryMax GENTLE F60056/10 Ref F60056/10
DryMax SOFT F60016/10 Ref F60016/10
DryMax SOFT F60015/10 Ref F60015/10
DryMax GENTLE F60053/10 Ref F60053/10
DryMax BORDER F50513/10 Ref F50513/10
DryMax SOFT F60013/10 Ref F60013/10
DryMax SOFT F60123/10 Ref F60123/10
DryMax GENTLE F60055/10 Ref F60055/10
DryMax SOFT F60018/10 Ref F60018/10
DryMax GENTLE F60057/10 Ref F60057/10
DryMax FOAM F60041/10 Ref F60041/10
DryMax BORDER F50511/10 Ref F50511/10
DryMax SOFT F60017/10 Ref F60017/10
Absorbest Super Foam F60045/10 Ref F60045/10
DryMax SOFT F60121/10 Ref F60121/10
DryMax BORDER F50514/10 Ref F50514/10
DryMax Soft F60125/10 Ref F60125/10
DryMax FOAM F60046/10 Ref F60046/10
FDA establishments
- Absorbest Ab Kisa Ostergotland · SE FEI 3008821638
What Absorbest AB makes
Absorbest AB manufactures hydrophilic-gel and foam-based exudate-absorbent dressings designed for wound care. Their products include non-antimicrobial variants such as DryMax SOFT, DryMax FOAM, DryMax BORDER, and Absorbest Super Foam, which are intended for managing fluid drainage from wounds.
These devices are classified as Class I under regulatory frameworks and are listed in the FDA’s Unique Device Identifier (UDI) database. The company operates from the United States, adhering to applicable medical device regulations for low-risk wound care products.
Frequently asked questions
What types of medical devices does Absorbest AB manufacture?
Absorbest AB specializes in exudate-absorbent dressings, specifically hydrophilic-gel and foam-based varieties. Their products are designed to manage fluid drainage from wounds and are non-antimicrobial. Examples include DryMax SOFT, DryMax FOAM, DryMax BORDER, and Absorbest Super Foam, all tailored for wound care applications.
Where is Absorbest AB based, and what does this mean for their regulatory compliance?
Absorbest AB is based in the United States. Since their devices fall under the FDA’s jurisdiction, the company must comply with U.S. medical device regulations. Their products are classified as Class I, which typically involves less stringent regulatory oversight compared to higher-risk devices, but they still must meet FDA requirements for safety and performance.
Which regulatory registries list Absorbest AB’s devices?
Absorbest AB’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices in the U.S. market, ensuring transparency and traceability for healthcare providers and regulators.
How are Absorbest AB’s devices classified under regulatory frameworks?
Absorbest AB’s exudate-absorbent dressings are classified as Class I devices. This classification is based on their intended use—low-risk wound care products that manage fluid drainage without antimicrobial properties. Class I devices generally require less regulatory scrutiny, but they must still comply with applicable safety and performance standards.
Information
- Country
- US
- DUNS number
- 631758273