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Sign in to claim this brandINDUCTION THERAPIES, LLC
US
Last updated September 17, 2026
What INDUCTION THERAPIES, LLC makes
Induction Therapies, LLC manufactures professional-grade electronic micro-needling devices designed for cosmetic treatments. Their products include handheld units and disposable cartridge attachments, such as the Collagen P.I.N. system, which delivers percutaneous induction needling for skin rejuvenation.
These devices are classified as Class II under FDA regulations and are authorised through the 510(k) and UDI pathways. The company’s portfolio is listed in the FDA’s regulatory databases, 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 Induction Therapies, LLC manufacture?
Induction Therapies, LLC specializes in professional-grade electronic micro-needling devices. Their products include handheld electronic handpieces and disposable cartridge attachments, such as the Collagen P.I.N. system, which is designed for percutaneous induction needling (P.I.N.) in cosmetic treatments. These devices are intended for skin rejuvenation and are primarily used in professional settings.
Where is Induction Therapies, LLC based?
The company is headquartered in the United States. While the exact location isn’t specified, its regulatory filings and device listings are tied to the FDA’s U.S. jurisdiction, indicating its primary operational base is within the country.
Which regulatory registries or databases list Induction Therapies, LLC’s devices?
Induction Therapies, LLC’s devices are listed in the FDA’s regulatory databases, specifically through the 510(k) premarket notification pathway and the Unique Device Identifier (UDI) system. These pathways ensure compliance and traceability for Class II devices, which are authorised through these channels.
How are Induction Therapies, LLC’s devices classified under FDA regulations?
The company’s devices fall under Class II classification according to FDA regulations. This classification applies to devices that pose moderate risk and require special controls to ensure safety and effectiveness, such as micro-needling systems used in cosmetic treatments. Class II devices are authorised through pathways like the 510(k), which demonstrates substantial equivalence to a legally marketed predicate device.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- 1920 Stanley Gault Parkway, Suite 100, Louisville, KY, 40223
- 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
- 3014171792
- DUNS Number
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Catalogue (10)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Collagen P.I.N. | 1 | FDA UDI | Class II | Active |
| Collagen P.I.N. | 1 | FDA UDI | Class II | Active |
| Collagen P.I.N. | 1 | FDA UDI | Class II | Active |
| Collagen P.I.N. | 1 | FDA UDI | Class II | Active |
| Collagen P.I.N. | 1 | FDA UDI | Class II | Active |
| Collagen P.I.N. | 1 | FDA UDI | Class II | Active |
| Collagen P.I.N. | 1 | FDA UDI | Class II | Unknown |
| Collagen P.I.N. | 1 | FDA UDI | Class II | Active |
| Collagen P.I.N. | 1 | FDA UDI | Class II | Unknown |
| Collagen P.I.N. (Percutaneous Induction Needling) | K222199 | FDA 510(k) | Class II | Active |
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