Escada International, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Escada International, Inc. makes
Escada International, Inc. manufactures low-level laser therapy (LLLT) devices, including the TQ SOLO, SOLO PRO, and LS50 accessory, as well as the MR4 Multi Radiance Therapy System. The company also produces the TerraQuant MQ2000 laser therapy device in multiple configurations, such as the MQ2000 V.5 and HandyRX MQ2007, and integrates laser therapy with TENS units like the TQ-1TENS.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Terraquant MQ2000 Laser Therapy Device Ref K043055
Regimes: 510(k) Registry: 510(k)Terraquant MQ2000 V. 5 And Handyrx MQ2007 Lasers Ref K061614
Regimes: 510(k) Registry: 510(k)Terraquant MQ2000 V.5 With The Tq-1TENS Ref K071445
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Escada International, Inc. have in the registry?
The registry currently lists 4 devices for Escada International, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Escada International, Inc.'s devices?
Among its 4 most recently registered devices, Escada International, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Escada International, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Escada International, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Escada International, Inc. in the registry?
The most recently registered devices listed for Escada International, Inc. include TQ SOLO AND SOLO PRO AND LS50 ACCESSORY AND MR4 MULTI RADIANCE THERAPY SYSTEM, TERRAQUANT MQ2000 LASER THERAPY DEVICE, TERRAQUANT MQ2000 V. 5 AND HANDYRX MQ2007 LASERS and TERRAQUANT MQ2000 V.5 WITH THE TQ-1TENS.