PainAway
by Multi Radiance Medical 2 variants
PainAway (600-200) is a Class II device made by Multi Radiance Medical, listed in FDA GUDID since 7 Sep 2021 (UDI-DI 00852556007336), registry data as of 31 May 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00852556007336 | Date7 Sep 2021 | StatusListed |
Official records
- AccessGUDID record 00852556007336
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic name
- Musculoskeletal infrared phototherapy unit, non-wearable
- Model / Ref / Catalog
- PainAway, 600-200
- Primary DI / UDI-DI
- 00852556007336
- FDA product code
- ILY
- GMDN term
- Musculoskeletal infrared phototherapy unit, non-wearable
- Device class
- Class II
- Regulation number
- 890.5500
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code ILY (Lamp, Infrared, Therapeutic Heating).
- PALOMAR LIGHTCUBE by Palomar Medical Products, Inc.
- M8 F9000247 by ASA SRL
- SACRED CRANE TDP LAMP, MODELS CQ-27, CQ-12, CQ-36 by United Pacific Co., Ltd.
- VARAYA AR, VARAYA SPORT by Varaya Photoceuticals, LLC
- BIOLIGHT BIODYNAM by Biolight AB
- VECTRA GENISYS (MODULE & TRANSPORTABLE) AND INTELECT XT (MODULE & TRANSPORTABLE) LASER SYSTEMS by Chattanooga Group, Inc.
- iLux LF V10 1LFV10 by MECTRONIC MEDICALE SRL
- CL10009 IR LASER by Curae'Lase, Inc.
- AKLARUS PHOTOTHERAPY SYSTEM by Hill Laboratories
- POWERLASER by Powermedic ApS