RecallHawk

Dentsply Sirona Titanium Bases system

Dentsply Sirona

Summary

Dentsply Sirona received 510(k) clearance for Dentsply Sirona Titanium Bases system, a NHA device. Cleared on 2025-04-30.

Details

Source

510(k) Clearance

External ID

K250295

Action Date

2025-04-30

Status

Traditional

Category

device

Product Code

NHA

Product Description

Dentsply Sirona Titanium Bases system. Product code: NHA.

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. Dentsply Sirona has received 20 total clearances in our database.

Dentsply Sirona has 20 FDA actions in our database, including 20 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 Dentsply Sirona have FDA actions?

Dentsply Sirona has 20 FDA actions in our database, including 0 recalls and 20 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K250295" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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