Alexandrite and Nd:YAG Laser models CANLASE and TORLASE
Canadian Pioneer Medical Technology Corporation (Cpmt Laser)
Summary
Canadian Pioneer Medical Technology Corporation (Cpmt Laser) received 510(k) clearance for Alexandrite and Nd:YAG Laser models CANLASE and TORLASE, a GEX device. Cleared on 2022-11-17.
Details
Source
510(k) Clearance
External ID
K222673
Action Date
2022-11-17
Status
Traditional
Category
device
Product Code
GEX
Product Description
Alexandrite and Nd:YAG Laser models CANLASE and TORLASE. 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. Canadian Pioneer Medical Technology Corporation (Cpmt Laser) has received 2 total clearances in our database.
Canadian Pioneer Medical Technology Corporation (Cpmt Laser) 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 Canadian Pioneer Medical Technology Corporation (Cpmt Laser) have FDA actions?
Canadian Pioneer Medical Technology Corporation (Cpmt Laser) 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 "K222673" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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