Therabody

FDA UDI

Class II (US FDA UDI)

by Therabody, Inc.

Identity

Trade Name: Therabody FDA UDI
Generic Name: Sequential venous compression system inflator FDA UDI
Device Name: RecoveryAir JetBoots Pro is a pair of pneumatic compression boots that incorporate vibration and IR technologies. These new features will enhance recovery of legs throughout their combination in different preset programs. The device is designed to work in pairs with a master boot, with a main control panel, and a dummy boot. Additionally, it will be Bluetooth enabled to connect with the Therabody App where user can access to more settings, presets, and track overall usage FDA UDI
Model / Reference: JetBoots PRO Plus Short FDA UDI
Description: RecoveryAir JetBoots Pro is a pair of pneumatic compression boots that incorporate vibration and IR technologies. These new features will enhance recovery of legs throughout their combination in different preset programs. The device is designed to work in pairs with a master boot, with a main control panel, and a dummy boot. Additionally, it will be Bluetooth enabled to connect with the Therabody App where user can access to more settings, presets, and track overall usage FDA UDI

Identifiers

Primary DI / UDI-DI: 00840295405568 FDA UDI
FDA Product Code: ILY FDA UDI
IRO FDA UDI
IRP FDA UDI
GMDN Term: Sequential venous compression system inflator FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 890.5500 FDA UDI
890.5975 FDA UDI
890.5650 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

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Single Use

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Implantable

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Contains Latex

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Prescription Use

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Over-the-Counter

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Convenience Kit

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Combination Product

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HCT/P

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Premarket Exempt

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Lot / Batch Number

Yes

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Serial Number

Yes

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Expiration Date

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Manufacturing Date

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Category: Sequential venous compression system inflator

Therabody by Therabody, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Bio Compression Systems Sequential Circulator Model SC-3008-IS — BIO COMPRESSION SYSTEMS, INC. · Class II
Air Relax Classic Model AR-2.0 Leg Recovery System - Size 2 — Maxstar Industrial Co., Ltd. · Class II
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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Therabody, Inc.

Sources (1)

FDA UDI 4d546fbc-15df-4baf-aae5-a8a95d634853 33 fields · synced May 30, 2026