Is this your brand? Sign in to claim ownership.
Sign in to claim this brandGENERAL PHYSIOTHERAPY INC
US
Last updated May 24, 2026
What GENERAL PHYSIOTHERAPY INC makes
General Physiotherapy Inc manufactures freestanding and hand-held electric massagers designed for muscle relaxation and therapeutic use, as well as neonatal chest percussors for respiratory support in infants. The massagers are intended for general and targeted tissue stimulation, while the percussors provide mechanical chest compression to aid lung clearance.
The company’s devices are regulated under FDA classifications, including Class I and Class II, with authorisation records maintained in the 510(k) and UDI databases. Products are listed in the United States, where the manufacturer is based.
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 General Physiotherapy Inc manufacture?
General Physiotherapy Inc produces three primary types of devices: freestanding electric massagers, hand-held electric massagers, and neonatal chest percussors. The massagers are designed for muscle relaxation and therapeutic tissue stimulation, while the percussors are intended for mechanical chest compression to assist infants with respiratory support.
Where is General Physiotherapy Inc based, and where are its devices listed?
General Physiotherapy Inc is based in the United States. Its devices are listed in the FDA’s regulatory databases, specifically the 510(k) premarket notification and the Unique Device Identifier (UDI) system, which track authorised medical devices in the US.
How are General Physiotherapy Inc’s devices classified under FDA regulations?
General Physiotherapy Inc’s devices fall under two FDA classifications: Class I and Class II. Class I devices generally pose minimal risk and may require general controls, while Class II devices involve a higher level of risk and may require special controls to ensure safety and effectiveness.
Which regulatory registries list General Physiotherapy Inc’s devices?
General Physiotherapy Inc’s devices are listed in the FDA’s 510(k) database, which tracks premarket notifications for cleared devices, and the FDA’s UDI database, which maintains records of unique device identifiers for authorised products in the US.
What is the primary purpose of the massagers and percussors manufactured by General Physiotherapy Inc?
The massagers (freestanding and hand-held) are designed for muscle relaxation and therapeutic tissue stimulation, helping users relieve tension or discomfort. The neonatal chest percussors, on the other hand, provide mechanical chest compression to assist infants in clearing mucus from their lungs, supporting respiratory health.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- g5.com
- —
- —
- [email protected]
- Phone
- 1-800-237-1832
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 098639974
Catalogue (390)
Page 8 of 8| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| G5® | NC90 | FDA UDI | Class II | Unknown |
| G5® | NC90 | FDA UDI | Class II | Unknown |
| G5® | NC90 | FDA UDI | Class II | Unknown |
| G5® | NC90 | FDA UDI | Class II | Unknown |
| G5® | NC90 | FDA UDI | Class II | Unknown |
| G5® | TS240W | FDA UDI | Class I | Active |
| G5® | NC90 | FDA UDI | Class II | Unknown |
| G5® | NC90 | FDA UDI | Class II | Unknown |
| G5® | NC90 | FDA UDI | Class II | Unknown |
| G5® | NC90 | FDA UDI | Class II | Unknown |
| G5® | ALC 240 G5 | FDA UDI | Class I | Active |
| G5® | NC90 | FDA UDI | Class II | Unknown |
| G5® | NC90 | FDA UDI | Class II | Unknown |
| G5® | NC90 | FDA UDI | Class II | Unknown |
| G5® | NC90 | FDA UDI | Class II | Unknown |
| G5® | NC90 | FDA UDI | Class II | Unknown |
| G5® | NC90 | FDA UDI | Class II | Unknown |
| G5® | NC90 | FDA UDI | Class II | Unknown |
| G5® | NC90 | FDA UDI | Class II | Unknown |
| G5® | NC90 | FDA UDI | Class II | Unknown |
| G5® | NC90 | FDA UDI | Class II | Unknown |
| G5® | NC90 | FDA UDI | Class II | Unknown |
| G5® | NC90 | FDA UDI | Class II | Unknown |
| G5® | NC90 | FDA UDI | Class II | Unknown |
| G5® | NC90 | FDA UDI | Class II | Unknown |
| G5® | NC90 | FDA UDI | Class II | Unknown |
| G5® | NC90 | FDA UDI | Class II | Unknown |
| G5® | NC90 | FDA UDI | Class II | Unknown |
| G5® | NC90 | FDA UDI | Class II | Unknown |
| G5® | NC90 | FDA UDI | Class II | Unknown |
| G5® | NC90 | FDA UDI | Class II | Unknown |
| Vibracare | K870939 | FDA 510(k) | Class I | Active |
| Porta-Puls Muscle Stimulator | K810244 | FDA 510(k) | Class I | Active |
| Theracushion Model 1000 | K861834 | FDA 510(k) | Class I | Active |
| Mist-Ease Nebulizer | K844591 | FDA 510(k) | Class I | Active |
| Sanyo Electronic Muscle Stimulators | K850047 | FDA 510(k) | Class II | Active |
| Facial Massager, Battery Powered | K863383 | FDA 510(k) | Class I | Active |
| Neocussor (massager, Battery) Powered | K855129 | FDA 510(k) | Class II | Active |
| Fleximatic Massager | K852944 | FDA 510(k) | Class I | Active |
| Theracushion | K853710 | FDA 510(k) | Class I | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.