Diode Laser System (LaserPro D 980); Diode Laser System (LaserPro D 810); Diode Laser System (Aurolance 980); Diode Lase
Summary
Jiangxi Medex Technology Co., Ltd. received 510(k) clearance for Diode Laser System (LaserPro D 980); Diode Laser System (LaserPro D 810); Diode Laser System (Aurolance 980); Diode Laser System (Aurolance 810); Diode Laser System (Aurolance AM), a GEX device. Cleared on 2024-12-26.
Details
Source
510(k) Clearance
External ID
K243141
Action Date
2024-12-26
Status
Traditional
Category
device
Product Code
GEX
Product Description
Diode Laser System (LaserPro D 980); Diode Laser System (LaserPro D 810); Diode Laser System (Aurolance 980); Diode Laser System (Aurolance 810); Diode Laser System (Aurolance AM). 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. Jiangxi Medex Technology Co., Ltd. has received 2 total clearances in our database.
Jiangxi Medex Technology Co., Ltd. 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 Jiangxi Medex Technology Co., Ltd. have FDA actions?
Jiangxi Medex Technology Co., Ltd. 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 "K243141" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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