SOGA Lasers therapy system family of Aurora handpiece (Aurora-S); SOGA Lasers therapy system family of the Dental diode
Summary
Shenzhen Soga Technology Co., Ltd. received 510(k) clearance for SOGA Lasers therapy system family of Aurora handpiece (Aurora-S); SOGA Lasers therapy system family of the Dental diode laser ( ILaser III Pro), a NVK device. Cleared on 2026-05-19.
Details
Source
510(k) Clearance
External ID
K253309
Action Date
2026-05-19
Status
Traditional
Category
device
Product Code
NVK
Product Description
SOGA Lasers therapy system family of Aurora handpiece (Aurora-S); SOGA Lasers therapy system family of the Dental diode laser ( ILaser III Pro). Product code: NVK.
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. Shenzhen Soga Technology Co., Ltd. has received 3 total clearances in our database.
Shenzhen Soga Technology Co., Ltd. has 3 FDA actions in our database, including 3 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 Shenzhen Soga Technology Co., Ltd. have FDA actions?
Shenzhen Soga Technology Co., Ltd. has 3 FDA actions in our database, including 0 recalls and 3 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "K253309" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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