# K242940: Xrecovery (XR-001)

- Pathway: 510(k) (Traditional)
- Applicant: Shenzhen Xinrun Electric Appliances Co, Ltd.
- Decided: Nov 14, 2024 after 50 days
- Product code: IRP (Massager, Powered Inflatable Tube)
- Device class: 2
- Regulation: 21 CFR 890.5650
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K944567 (1995). 14 ancestors in all.
No later device cites it as a predicate yet.
0 of 15 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K183702: Polar Care Wave, Breg, Inc. (2019) Summary page 5.

## Indications for use
The Xrecovery is intended to treat post-surgical and acute injuries to reduce edema, swelling, and pain where cold and compression are indicated. It is intended to be used by or on the order of licensed healthcare professionals in hospitals, outpatient clinics, athletic training settings, or home settings.

Source page: https://510kreport.com/device/K242940
Methodology: https://510kreport.com/methodology