RecallHawk

Summary

Shenzhenshi Sincoheren S&T Development Co., Ltd. received 510(k) clearance for LED Spectrum therapy instrument, a GEX device. Cleared on 2023-09-20.

Details

Source

510(k) Clearance

External ID

K231894

Action Date

2023-09-20

Status

Traditional

Category

device

Product Code

GEX

Product Description

LED Spectrum therapy instrument. Product code: GEX.

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. Shenzhenshi Sincoheren S&T Development Co., Ltd. has received 2 total clearances in our database.

Shenzhenshi Sincoheren S&T Development Co., Ltd. has 2 FDA actions in our database, including 2 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 Shenzhenshi Sincoheren S&T Development Co., Ltd. have FDA actions?

Shenzhenshi Sincoheren S&T Development Co., Ltd. has 2 FDA actions in our database, including 0 recalls and 2 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K231894" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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