# K211745: RecoveryAir PRO

- Pathway: 510(k) (Traditional)
- Applicant: Theragun, Inc.
- Decided: Oct 4, 2021 after 119 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: 1 generation back to K140519 (2014). 1 ancestor in all.
4 later devices descend from it; 3 cite it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K140519: Recovery Pump 737R, Mego Afek AC, Ltd. (2014) Summary page 4.

## Most influential descendants
- K241256: JetBoots PRO Plus (2024), 1 descendant of its own
- K242140: Air Compression Leg Massager (K-705) (2025), 0 descendants of its own
- K243206: Air compression massager (ACM-PLUS-A1, ACM-PLUS-A2, ACM-PLUS-A3, ACM-PLUS-A4, ACM-PLUS-A5, ACM-PLUS-A6) (2025), 0 descendants of its own
- K233238: Air Pressure Therapy System (Model:VU-IPC4M) (2024), 0 descendants of its own

## Indications for use
The RecoveryAir PRO is an air compression therapy device intended to provide graduated pressure to compression garments. The RecoveryAir PRO is indicated for the temporary relief of minor muscle aches and pains, and for temporary increase in circulation to the treated areas in people who are in good health. The RecoveryAir PRO simulates kneading and stroking of tissues by using an inflatable garment.

Source page: https://510kreport.com/device/K211745
Methodology: https://510kreport.com/methodology