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Sign in to claim this brandAbsorbest AB
US
Last updated May 23, 2026
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.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
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.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 631758273
Catalogue (30)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| DryMax SOFT | F60014/10 | FDA UDI | Class I | Active |
| Absorbest Super Foam | F60046/10 | FDA UDI | Class I | Active |
| DryMax SOFT | F60011/10 | FDA UDI | Class I | Active |
| DryMax FOAM | F60044/10 | FDA UDI | Class I | Active |
| DryMax BORDER | F50515/10 | FDA UDI | Class I | Active |
| DryMax FOAM | F60045/10 | FDA UDI | Class I | Active |
| Absorbest Super Foam | F60041/10 | FDA UDI | Class I | Active |
| DryMax FOAM | F60043/10 | FDA UDI | Class I | Active |
| DryMax SOFT | F60019/10 | FDA UDI | Class I | Active |
| DryMax SOFT | F60012/10 | FDA UDI | Class I | Active |
| Absorbest Super Foam | F60044/10 | FDA UDI | Class I | Active |
| Absorbest Super Foam | F60043/10 | FDA UDI | Class I | Active |
| DryMax GENTLE | F60056/10 | FDA UDI | Class I | Active |
| DryMax SOFT | F60016/10 | FDA UDI | Class I | Active |
| DryMax SOFT | F60015/10 | FDA UDI | Class I | Active |
| DryMax GENTLE | F60053/10 | FDA UDI | Class I | Active |
| DryMax BORDER | F50513/10 | FDA UDI | Class I | Active |
| DryMax SOFT | F60013/10 | FDA UDI | Class I | Active |
| DryMax SOFT | F60123/10 | FDA UDI | Class I | Active |
| DryMax GENTLE | F60055/10 | FDA UDI | Class I | Active |
| DryMax SOFT | F60018/10 | FDA UDI | Class I | Active |
| DryMax GENTLE | F60057/10 | FDA UDI | Class I | Active |
| DryMax FOAM | F60041/10 | FDA UDI | Class I | Active |
| DryMax BORDER | F50511/10 | FDA UDI | Class I | Active |
| DryMax SOFT | F60017/10 | FDA UDI | Class I | Active |
| Absorbest Super Foam | F60045/10 | FDA UDI | Class I | Active |
| DryMax SOFT | F60121/10 | FDA UDI | Class I | Active |
| DryMax BORDER | F50514/10 | FDA UDI | Class I | Active |
| DryMax Soft | F60125/10 | FDA UDI | Class I | Active |
| DryMax FOAM | F60046/10 | FDA UDI | Class I | Active |
Related Companies
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Absorbest Ab Kisa Ostergotland · SE FEI 3008821638