RecallHawk

Surgic Pro2 (Surgic Pro2 OPT), Surgic Pro2 (Surgic Pro2 NON-OPT)

Nakanishi, Inc.

Summary

Nakanishi, Inc. received 510(k) clearance for Surgic Pro2 (Surgic Pro2 OPT), Surgic Pro2 (Surgic Pro2 NON-OPT), a EBW device. Cleared on 2024-06-20.

Details

Source

510(k) Clearance

External ID

K233117

Action Date

2024-06-20

Status

Traditional

Category

device

Product Code

EBW

Product Description

Surgic Pro2 (Surgic Pro2 OPT), Surgic Pro2 (Surgic Pro2 NON-OPT). Product code: EBW.

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. Nakanishi, Inc. has received 12 total clearances in our database.

Nakanishi, Inc. has 12 FDA actions in our database, including 12 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 Nakanishi, Inc. have FDA actions?

Nakanishi, Inc. has 12 FDA actions in our database, including 0 recalls and 12 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K233117" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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