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Sign in to claim this brandADVANCED MEDICAL SOLUTIONS LIMITED
US
Last updated May 23, 2026
What ADVANCED MEDICAL SOLUTIONS LIMITED makes
Advanced Medical Solutions Limited manufactures a range of wound care dressings, including hydrophilic-gel and non-gel exudate-absorbent products, some of which incorporate antimicrobial properties. Their portfolio also includes reusable antimicrobial fabrics for skin friction and moisture control, as well as non-antimicrobial wound hydrogels and woven gauze pads designed for single-use applications.
The company’s devices are regulated under FDA classifications spanning Class I, Class II, Class III, and Unclassified (U), with submissions including 510(k), PMA, and UDI registrations. Their products are listed in the US under FDA regulatory pathways, and the manufacturer is based in the United States.
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 Advanced Medical Solutions Limited primarily manufacture?
Advanced Medical Solutions Limited specializes in wound care dressings. Their portfolio includes exudate-absorbent dressings, such as hydrophilic-gel and non-gel varieties, some of which have antimicrobial properties. They also produce reusable antimicrobial fabrics for skin friction and moisture control, as well as non-antimicrobial wound hydrogels and woven gauze pads. These products are designed for single-patient use or reusable applications depending on the category.
Where is Advanced Medical Solutions Limited based, and how does this affect their regulatory oversight?
Advanced Medical Solutions Limited is based in the United States. Since they operate within the US, their devices are regulated under the FDA’s regulatory framework. The company’s products are listed in US registries such as 510(k), PMA, and UDI, reflecting compliance with FDA requirements for medical devices in the country.
Which regulatory registries list devices manufactured by Advanced Medical Solutions Limited?
Devices from Advanced Medical Solutions Limited are listed in the FDA’s regulatory registries, including the 510(k) pathway for Class II devices, PMA (Premarket Approval) for Class III devices, and UDI (Unique Device Identification) registrations. These pathways ensure traceability and compliance with US medical device regulations.
How are the devices produced by Advanced Medical Solutions Limited classified under FDA regulations?
The devices manufactured by Advanced Medical Solutions Limited fall under multiple FDA classifications: Class I (generally low-risk), Class II (requires special controls), Class III (high-risk requiring PMA), and Unclassified (U) devices. The classification depends on factors like the device’s intended use, risk level, and regulatory history, determining the submission pathway required for market authorization.
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
- 770434090
Catalogue (225)
Page 5 of 5| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Gemcore360 | Hydrocolloid Foam Backed | FDA UDI | Class I | Unknown |
| ActivHeal | Alginate | FDA UDI | Class I | Active |
| Tegaderm | Hydrogel | FDA UDI | Class I | Unknown |
| McKesson | Moisture Wicking Fabric Ag | FDA UDI | Class I | Active |
| ActivHeal | PHMB Foam Antimicrobial Non-Border, Non-Adhesive | FDA UDI | U | Active |
| ActivHeal | High Performance Dressing | FDA UDI | Class I | Active |
| Gemcore360 | Hydrocolloid Film Backed | FDA UDI | Class I | Unknown |
| Gemcore360 | Silicone Foam Adhesive Border | FDA UDI | Class I | Unknown |
| Tegaderm | Alginate | FDA UDI | Class I | Active |
| Biatain | Alginate Ag | FDA UDI | U | Active |
| Biatain | Alginate Ag | FDA UDI | U | Active |
| Tegaderm | Alginate | FDA UDI | Class I | Active |
| Gemcore360 | PHMB Foam Antimicrobial Non-Border, Non-Adhesive | FDA UDI | U | Unknown |
| Silver Pu Antibacterial Foam Dressing - Non Adherent And Island | K091013 | FDA 510(k) | U | Active |
| Silver Alginate 11 Wound Dressing | K090453 | FDA 510(k) | U | Active |
| Non-Adherent Antimicrobial Alginate Dressing, Silvercel Non-Adherent Antimicrobial Alginate Dressing | K081363 | FDA 510(k) | U | Active |
| Silver Alginate Iv Antimicrobial Wound Dressing | K080503 | FDA 510(k) | U | Active |
| Silver Alginate Ii Wound Dressing | K070581 | FDA 510(k) | U | Active |
| LiquiBand Plus | K183570 | FDA 510(k) | Class II | Active |
| Silver Antimicrobial Wound Gel | K110458 | FDA 510(k) | U | Active |
| Modification To Silver Alginate Ii Wound Dressing | K063173 | FDA 510(k) | U | Active |
| Antimicrobial Silicone PHMB Foam Wound Dressing | K223310 | FDA 510(k) | U | Active |
| Silver Antimicrobial Wound Gel | K073197 | FDA 510(k) | U | Active |
| LiquiBand XL | K211878 | FDA 510(k) | Class II | Active |
| LIQUIFIX FIX8 Hernia Mesh Fixation (HMF) Device, LIQUIFIX Precision Open Hernia Mesh Fixation Device | P220024 | FDA PMA | Class III | Active |
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Advanced Medical Solutions Ltd WINSFORD Cheshire East · GB FEI 3003080333