Is this your brand? Sign in to claim ownership.
Sign in to claim this brandHovertech International
United States·US-MF-000008435
Last updated May 24, 2026
What Hovertech International makes
Hovertech International manufactures powered patient transfer systems, including slings and mats designed for single-use or reusable applications, as well as air-powered patient lifting belts and harnesses. Their product line also includes manual patient lifting belts and air compressors for medical use, such as the HoverSling and SizeWise Matt. These devices are intended for use in clinical settings to assist with patient mobility and handling.
The company’s devices are classified under Class I and Class II regulations, with listings in the EU’s EUDAMED database and the FDA’s Unique Device Identifier (UDI) system. Their products are intended for global markets, including the European Economic Area and the United States, where applicable regulatory requirements apply.
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 Hovertech International manufacture?
Hovertech International specializes in devices that assist with patient mobility and handling. Their primary products include powered patient transfer systems, such as slings and mats (like the HoverSling and SizeWise Matt), which are designed for single-use or reusable applications. They also produce air-powered patient lifting belts/harnesses and medical device air compressors (e.g., HoverTech Air Supply). These devices are engineered for clinical environments to support safe and efficient patient transfers.
Where is Hovertech International based, and where are their devices listed?
Hovertech International is based in the United States. Their devices are registered in two key regulatory databases: EUDAMED (the European database for medical devices) and the FDA’s Unique Device Identifier (UDI) system in the U.S. These listings ensure compliance with regulatory requirements in the European Economic Area and United States, where applicable.
How are Hovertech International’s devices classified under medical device regulations?
Hovertech International’s devices fall under Class I and Class II classifications. The classification determines regulatory oversight and requirements for market authorization. For example, powered patient transfer systems (like slings or mats) are often Class II due to their role in patient safety and risk mitigation, while simpler air compressors or manual belts may qualify as Class I. Classification depends on factors like intended use, risk, and design complexity as defined by regional regulations.
Are Hovertech International’s devices intended for global markets, and how does that affect their regulatory status?
Yes, Hovertech International’s devices are designed for global markets, including the European Economic Area (EEA) and the United States. This means their products must comply with EU MDR (Medical Device Regulation) requirements for EEA markets and FDA regulations for U.S. sales. Each region has its own classification system (e.g., EU’s Class I/II vs. FDA’s Class I/II/III), so devices may undergo separate evaluations or registrations depending on the destination. Their listings in EUDAMED and FDA UDI reflect this global approach.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- United States
- Address
- 4482, Innovation Way , Allentown, United States
- Website
- www.HoverMatt.com
- —
- —
- [email protected]
- Phone
- 6106949600
- PRRC Contact
- Susan Pavelko
- EUDAMED SRN
- US-MF-000008435
- FDA FEI Number
- —
- DUNS Number
- 942139841
Catalogue (111)
Page 1 of 3| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| HoverSling | HMSLING-39-B | FDA UDI | Class II | Active |
| Single Patient Use HoverMatt | HM39SPU-TVA-B | FDA UDI | Class II | Active |
| Single Patient Use HoverMatt | RGMT50FL-REG | FDA UDI | Class II | Active |
| HoverMatt SPU Plus HoverCover | HMHC-34 | FDA UDI | Class II | Active |
| HoverTech Air Supply | HTAIR2356 | FDA UDI | Class II | Active |
| SizeWise Matt | SW50HS | FDA UDI | Class II | Active |
| Single Patient Use HoverMatt | HM50SPU-TVA | FDA UDI | Class II | Active |
| Single Patient Use HoverMatt | RGMT34FL-REG | FDA UDI | Class II | Active |
| Single Patient Use HoverMatt | HM34SPU-LNK-TVA-B | FDA UDI | Class II | Active |
| Single Patient Use HoverMatt | HM34SPU-HLF | FDA UDI | Class II | Active |
| Single Patient Use HoverMatt | HM34SPU | FDA UDI | Class II | Active |
| Single Patient Use HoverMatt | HM39SPU | FDA UDI | Class II | Active |
| Single Patient Use HoverMatt | HM50SPU | FDA UDI | Class II | Active |
| Single Patient Use HoverMatt | HM50SPU-LNK-TVA-B | FDA UDI | Class II | Active |
| HoverSling Repositiong Sling-TVA | HMSLING-50RS-TVA-B | FDA UDI | Class II | Active |
| HoverTech Air Supply | HTAIR1000 | FDA UDI | Class II | Active |
| HoverMatt | HM28DC | FDA UDI | Class II | Active |
| SizeWise Matt | SW34HS | FDA UDI | Class II | Active |
| HoverSling Repositiong Sling-TVA | HMSLING-39RS-TVA-B | FDA UDI | Class II | Active |
| Single Patient Use HoverMatt | RGMT39FL-REG | FDA UDI | Class II | Active |
| Single Patient Use HoverMatt | HM34SPU-TVA | FDA UDI | Class II | Active |
| HoverSling | HMSLING-39 | FDA UDI | Class II | Active |
| Single Patient Use HoverMatt | HM39SPU-LNK-TVA-B | FDA UDI | Class II | Active |
| Single Patient Use HoverMatt | HM34RPSPU | FDA UDI | Class II | Active |
| Single Patient Use HoverMatt | HM39SPU-HLF | FDA UDI | Class II | Active |
| HoverMatt SPU Plus HoverCover | HMHC-39 | FDA UDI | Class II | Active |
| Single Patient Use HoverMatt | HM50SPU-TVA-B | FDA UDI | Class II | Active |
| Single Patient Use HoverMatt | HM39SPU-HLF-TVA | FDA UDI | Class II | Active |
| Single Patient Use HoverMatt | HM50RPSPU | FDA UDI | Class II | Active |
| Single Patient Use HoverMatt | HM34SPU-HLF-TVA-B | FDA UDI | Class II | Active |
| SizeWise Matt | SW39HS | FDA UDI | Class II | Active |
| HoverMatt | HMSL34DC | FDA UDI | Class II | Active |
| HoverTech Air Supply | HTAIR1200 | FDA UDI | Class II | Active |
| Single Patient Use HoverMatt | HM34SPU-Split | FDA UDI | Class II | Active |
| AirWedge | HTPP-200 | FDA UDI | Class II | Active |
| Single Patient Use HoverMatt | HM39SPU-HLF-TVA-B | FDA UDI | Class II | Active |
| HoverSling | HMSLING-50 | FDA UDI | Class II | Active |
| Single Patient Use HoverMatt | RGMT39HLF-REG | FDA UDI | Class II | Active |
| HoverSling | HMSLING-50-B | FDA UDI | Class II | Active |
| HoverMatt | HM28HS | FDA UDI | Class II | Active |
| Single Patient Use HoverMatt | HM39RPSPU | FDA UDI | Class II | Active |
| HoverSling | HMSLING-34 | FDA UDI | Class II | Active |
| Single Patient Use HoverMatt | RGMT34HLF-REG | FDA UDI | Class II | Active |
| Single Patient Use HoverMatt | HM34SPU-HLF-TVA | FDA UDI | Class II | Active |
| Single Patient Use HoverMatt | HM39RPSPU-HLF | FDA UDI | Class II | Active |
| Single Patient Use HoverMatt | HM34SPU-TVA-B | FDA UDI | Class II | Active |
| SizeWise Air Supply | SW400AIR | FDA UDI | Class II | Active |
| Single Patient Use HoverMatt | HM34RPSPU-HLF | FDA UDI | Class II | Active |
| HoverTech Air Supply | AIR200G | FDA UDI | Class II | Active |
| HoverTech Air Supply | AIR400G | FDA UDI | Class II | Active |
Related Companies
Authorised Representatives
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.