VINScreen Urine Drug Test Cup; VINScreen Urine Drug Home Test Cup
Summary
Advin Biotech, Inc. received 510(k) clearance for VINScreen Urine Drug Test Cup; VINScreen Urine Drug Home Test Cup, a NFT device. Cleared on 2025-10-09.
Details
Source
510(k) Clearance
External ID
K252867
Action Date
2025-10-09
Status
Traditional
Category
device
Product Code
NFT
Product Description
VINScreen Urine Drug Test Cup; VINScreen Urine Drug Home Test Cup. Product code: NFT.
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.
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 Advin Biotech, Inc. have FDA actions?
This is the only FDA action we have on record for Advin Biotech, Inc. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "K252867" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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