IPG Medical Family of Thulium Fiber Lasers, Surgical Fibers, and Accessories
Summary
Ipg Medical Corporation received 510(k) clearance for IPG Medical Family of Thulium Fiber Lasers, Surgical Fibers, and Accessories, a GEX device. Cleared on 2024-03-21.
Details
Source
510(k) Clearance
External ID
K232568
Action Date
2024-03-21
Status
Traditional
Category
device
Product Code
GEX
Product Description
IPG Medical Family of Thulium Fiber Lasers, Surgical Fibers, and Accessories. Product code: GEX.
Company
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. Ipg Medical Corporation has received 2 total clearances in our database.
Ipg Medical Corporation 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 Ipg Medical Corporation have FDA actions?
Ipg Medical Corporation 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 "K232568" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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