RecallHawk

LensHooke CA1 Sperm Separation Device, LensHooke CA0 Sperm Separation Device

Bonraybio Co., Ltd.

Summary

Bonraybio Co., Ltd. received 510(k) clearance for LensHooke CA1 Sperm Separation Device, LensHooke CA0 Sperm Separation Device, a MQK device. Cleared on 2022-10-31.

Details

Source

510(k) Clearance

External ID

K221810

Action Date

2022-10-31

Status

Traditional

Category

device

Product Code

MQK

Product Description

LensHooke CA1 Sperm Separation Device, LensHooke CA0 Sperm Separation Device. Product code: MQK.

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. Bonraybio Co., Ltd. has received 3 total clearances in our database.

Bonraybio Co., Ltd. has 3 FDA actions in our database, including 3 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 Bonraybio Co., Ltd. have FDA actions?

Bonraybio Co., Ltd. has 3 FDA actions in our database, including 0 recalls and 3 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K221810" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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