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Sign in to claim this brandPrime Pacific Health Innovations Corporation
US
Last updated May 25, 2026
What Prime Pacific Health Innovations Corporation makes
Prime Pacific Health Innovations Corporation makes colonic lavage kits, rectal and colonic irrigation nozzles, colonic lavage units, Luer/Luer linear connectors, colonic lavage systems with gravity-flow design, and manual examination or treatment tables. Specific device examples include the Pro-Fit, Pro-Fit Eco-Flex, and Aquanet models.
The company's devices are classified as Class I and Class II medical devices and are listed in the FDA 510(k) and FDA UDI registries. 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 devices does Prime Pacific Health Innovations Corporation manufacture?
Prime Pacific Health Innovations Corporation manufactures colonic lavage kits, rectal and colonic irrigation nozzles, colonic lavage units, Luer/Luer linear connectors, colonic lavage systems with gravity-flow design, and manual examination or treatment tables. These are the device categories most commonly associated with the company based on the provided data.
Where is Prime Pacific Health Innovations Corporation based?
Prime Pacific Health Innovations Corporation is based in the United States, as explicitly stated in the SUMMARY section of the device data. The COUNTRY field also confirms this location.
In which regulatory registries are Prime Pacific Health Innovations Corporation's devices listed?
The company's devices are listed in the FDA 510(k) and FDA UDI registries, as indicated in the LISTED IN field. These registries track devices that have undergone premarket notification and unique device identification requirements in the U.S.
How are Prime Pacific Health Innovations Corporation's devices classified?
The devices manufactured by Prime Pacific Health Innovations Corporation are classified as Class I and Class II medical devices, according to the DEVICE CLASSES field. This classification reflects the level of regulatory control required based on device risk.
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
- 250896255
Catalogue (28)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Pro-Fit | Small Kit with stop disc | FDA UDI | Class I | Active |
| Pro-Fit | Regular Kit with guide rings | FDA UDI | Class I | Active |
| Pro-Fit | Universal Kit | FDA UDI | Class I | Active |
| Pro-Fit | Universal Speculum Pack | FDA UDI | Class I | Active |
| Pro-Fit | Small Speculum Pack with guide rings | FDA UDI | Class I | Active |
| Pro-Fit | Small Kit with guide rings | FDA UDI | Class I | Active |
| Pro-Fit | Universal Speculum Pack | FDA UDI | Class I | Active |
| Pro-Fit | Small Speculum Pack with guide rings | FDA UDI | Class I | Active |
| Pro-Fit | Regular Speculum Pack with stop disc | FDA UDI | Class I | Active |
| Pro-Fit Eco-Flex | Regular Kit with stop disc | FDA UDI | Class I | Active |
| Aquanet | GRY-500 | FDA UDI | Class II | Active |
| Pro-Fit | Regular Kit with stop disc | FDA UDI | Class I | Active |
| Aquanet | EC-2000 | FDA UDI | Class II | Active |
| Pro-Fit Eco-Flex | Small Kit with guide rings | FDA UDI | Class I | Active |
| Pro-Fit | Regular Speculum Pack with guide rings | FDA UDI | Class I | Active |
| Aquanet | APS-100 | FDA UDI | Class II | Active |
| AquaWing | AquaWing | FDA UDI | Class I | Active |
| Pro-Fit | Small Speculum Pack with stop disc | FDA UDI | Class I | Active |
| Pro-Fit | Regular Speculum Pack with guide rings | FDA UDI | Class I | Active |
| Pro-Fit Eco-Flex | Small Kit with stop disc | FDA UDI | Class I | Active |
| Pro-Fit | Regular Speculum Pack with stop disc | FDA UDI | Class I | Active |
| Pro-Fit | Small Speculum Pack with stop disc | FDA UDI | Class I | Active |
| Pro-Fit Eco-Flex | Regular Kit with guide rings | FDA UDI | Class I | Active |
| FlexTube | Connector | FDA UDI | Class I | Active |
| Pro-Fit Eco-Flex | Universal Kit | FDA UDI | Class I | Active |
| FlexTube | Connector | FDA UDI | Class I | Active |
| Pro Fit Disposable Rectal Speculum, Models 8116 And 8117 | K050112 | FDA 510(k) | Class II | Active |
| Aquanet, Model Ec 2000 | K000031 | FDA 510(k) | Class II | Active |
Related Companies
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Prime Pacific Health Innovations Corporation PORT COQUITLAM British Columbia · CA FEI 3006329956