510(k) · Radiology

Swoop® Portable MR Imaging® System

by Hyperfine, Inc.

Swoop® Portable MR Imaging® System is an AI-enabled medical device from Hyperfine, Inc. that the U.S. FDA cleared through 510(k) K251276 on May 21, 2025. Its lead review panel is Radiology and its primary product code is LNH (System, Nuclear Magnetic Resonance Imaging).

See also FDA-cleared AI radiology devices in 2025, all FDA AI clearances in 2025, top radiology AI devices.

Key facts

Submission numberK251276
Pathway510(k)
Date of final decision
Company (FDA list)Hyperfine, Inc.
Lead review panelRadiology
Primary product codeLNH — System, Nuclear Magnetic Resonance Imaging
Applicant (openFDA)Hyperfine, Inc.
Applicant locationGuilforf, CT, US
Device classClass 2
Regulation number21 CFR 892.1000
Decision codeSESE
Submission typeSpecial

Source: FDA AI-Enabled Medical Devices list and openFDA.

What this means

A 510(k) is a premarket submission showing the device is substantially equivalent to a legally marketed predicate device. A cleared 510(k) means FDA agreed with that equivalence. Swoop® Portable MR Imaging® System went through this pathway (K251276).

openFDA lists it as a Class 2 device under 21 CFR 892.1000. Class II devices are moderate risk and are subject to general and special controls.

Product code LNH covers 100 devices on the FDA AI list. By decision date, this device is #73 of 100 under that code. Hyperfine, Inc. has 12 AI-enabled devices on the list, and the Radiology panel accounts for 1,230 in total.

Being on this list doesn't describe how well the device works clinically. Check the FDA record for its indications for use.

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