Cryo Sport 2.0 (AVA 501)

FDA 510(k) K252396 · Avanutri Equipamentos DE Saúde

Substantially Equivalent

510(k) numberK252396

Submission

Device name
Cryo Sport 2.0 (AVA 501)
Applicant
Avanutri Equipamentos DE Saúde
Tres Rios, BR
Received
July 31, 2025
Decision date
May 29, 2026
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
IRP – Massager, Powered Inflatable Tube
Device class
Class II (moderate risk)
Regulation
21 CFR 890.5650
Specialty
Physical Medicine

Other 510(k)s with product code IRP

510(k)DeviceApplicantDecision
K260944ManaCold Compression SystemIRP · Traditional Manamed, LLC08/12/2026SE
K260529Air Compression Massager (HY-1165)IRP · Traditional Xiamen High Top Electronic Technology Co., Ltd.07/27/2026SE
K260948Air Compression Massager (EP30B001 I)IRP · Traditional Wavepulse (Xiamen) Healthcare Technology Co., Ltd.07/24/2026SE
K253919Cryo And Thermo Therapy SystemIRP · Traditional Xiamen Weiyou Intelligent Technology Co., Ltd.06/10/2026SE
K254200Air Compression Leg Massager (LF-FT001, LF-FT002-1, LF-FT003, LF-FT003-1, LF-FT004-1…IRP · Traditional Wenzhou Lingfeng Electronic Technology Co., Ltd.05/05/2026SE
K253064Air Pressure Therapy System (VU-IPC8M); Air Pressure Therapy System (VU-IPC6M); Air…IRP · Traditional Xiamen Weiyou Intelligent Technology Co., Ltd.04/30/2026SE
K252386Hot and Cold Compression System (A02-C-032)IRP · Traditional Chengdu Cryo-Push Medical Technology Co.,Ltd04/03/2026SE
K253076Cryopush Cold Compression Device (A02-P-001)IRP · Traditional Chengdu Cryo-Push Medical Technology Co.,Ltd04/02/2026SE
K251622Hand Massager (SM004D)IRP · Traditional Ningbo Zhenhai Yihao Electronic Technology Co.…01/28/2026SE
K251662Air Compression Therapy Device (ST-504); Air Compression Therapy Device (ST-505); Air…IRP · Traditional Shenzhen Future Electronic Co., Ltd.11/13/2025SE

Questions and answers

When was Cryo Sport 2.0 (AVA 501) cleared by the FDA?

Cryo Sport 2.0 (AVA 501) (K252396) received a 510(k) decision of Substantially Equivalent on May 29, 2026, 302 days after the submission was received.

What is the product code of K252396?

The FDA product code is IRP – Massager, Powered Inflatable Tube, a Class II (moderate risk) device regulated under 21 CFR 890.5650.