Identity
- Trade Name
- Ixyon XP F92 OA FDA UDI
- Generic Name
- Musculoskeletal/physical therapy laser, professional FDA UDI
- Device Name
- The device is emitting energy in the infrared spectrum to provide topical heating for the purpose of elevating tissue temperature for temporary relief of minor muscle and joint pain, muscle spasm, pain and stiffness associated with arthritis. It is also indicated for promoting relaxation of the muscle tissue and for temporarily increasing local blood circulation. FDA UDI
- Model / Reference
- 1IXF92OA FDA UDI
- Description
- The device is emitting energy in the infrared spectrum to provide topical heating for the purpose of elevating tissue temperature for temporary relief of minor muscle and joint pain, muscle spasm, pain and stiffness associated with arthritis. It is also indicated for promoting relaxation of the muscle tissue and for temporarily increasing local blood circulation. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08051499970765 FDA UDI
- FDA Product Code
- ILY FDA UDI
- GMDN Term
- Musculoskeletal/physical therapy laser, professional FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 890.5500 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Musculoskeletal/physical therapy laser, professional
Ixyon XP F92 OA by Mectronic Medicale Srl — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Musculoskeletal/physical therapy laser, professional.
- Dimed — Wuhan Dimed Laser Technology Co., Ltd. · Class II
- LZ30 — AVANT WELLNESS SYSTEMS INC · Class II
- EVRL — Erchonia Corporation · Class II
- Regenalase — IPG Medical Corporation · Class II
- Phoenix Thera-Lase system — Phoenix Thera-Lase Systems, LLC · Class II
- Diode Laser System Deep Tissue Handpiece — Biolase, Inc. · Class II
- MedX Rehab Portable Laser — MedX Health Corp · Class II
- Dimed — Wuhan Dimed Laser Technology Co., Ltd. · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Mectronic Medicale Srl
Sources (1)
- FDA UDI 95f65c43-2e7b-4a8d-99ac-9e8646046389 33 fields · synced Jun 8, 2026