RecallHawk

uMI Panvivo (uMI Panvivo LS); uMI Panvivo (uMI Panvivo); uMI Panvivo (uMI Panvivo S); uMI Panvivo (uMI Panvivo EX); uMI

Shanghai United Imaging Healthcare Co., Ltd.

Summary

Shanghai United Imaging Healthcare Co., Ltd. received 510(k) clearance for uMI Panvivo (uMI Panvivo LS); uMI Panvivo (uMI Panvivo); uMI Panvivo (uMI Panvivo S); uMI Panvivo (uMI Panvivo EX); uMI Panvivo (uMI Panvivo ES), a KPS device. Cleared on 2026-04-03.

Details

Source

510(k) Clearance

External ID

K260524

Action Date

2026-04-03

Status

Traditional

Category

device

Product Code

KPS

Product Description

uMI Panvivo (uMI Panvivo LS); uMI Panvivo (uMI Panvivo); uMI Panvivo (uMI Panvivo S); uMI Panvivo (uMI Panvivo EX); uMI Panvivo (uMI Panvivo ES). Product code: KPS.

Context & Analysis

A 510(k) clearance means the FDA determined this device is substantially equivalent to a legally marketed device. This is one of 403 device clearances issued this month. Shanghai United Imaging Healthcare Co., Ltd. has received 43 total clearances in our database.

Shanghai United Imaging Healthcare Co., Ltd. has 48 FDA actions in our database, including 5 recalls and 43 clearances.

Frequently Asked Questions

What does 510(k) clearance mean?

A 510(k) is an FDA premarket submission demonstrating that a device is substantially equivalent to a legally marketed device. It does NOT mean FDA approval — it means the device is cleared for marketing because it's similar enough to an existing cleared device. Most medical devices reach market via 510(k) rather than full PMA approval.

How often does Shanghai United Imaging Healthcare Co., Ltd. have FDA actions?

Shanghai United Imaging Healthcare Co., Ltd. has 48 FDA actions in our database, including 5 recalls and 43 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K260524" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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