RecallHawk

DX. Bond V Dental Bonding Adhesive

Sino-Dentex Co., Ltd.

Summary

Sino-Dentex Co., Ltd. received 510(k) clearance for DX. Bond V Dental Bonding Adhesive, a KLE device. Cleared on 2023-09-22.

Details

Source

510(k) Clearance

External ID

K232978

Action Date

2023-09-22

Status

Traditional

Category

device

Product Code

KLE

Product Description

DX. Bond V Dental Bonding Adhesive. Product code: KLE.

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.

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 Sino-Dentex Co., Ltd. have FDA actions?

This is the only FDA action we have on record for Sino-Dentex Co., Ltd. in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K232978" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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