STERRAD 100NX Sterilization System with ALLClear Technology (10104)
Summary
Advanced Sterilization Products, Inc. received 510(k) clearance for STERRAD 100NX Sterilization System with ALLClear Technology (10104), a MLR device. Cleared on 2026-04-15.
Details
Source
510(k) Clearance
External ID
K252843
Action Date
2026-04-15
Status
Traditional
Category
device
Product Code
MLR
Product Description
STERRAD 100NX Sterilization System with ALLClear Technology (10104). Product code: MLR.
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. Advanced Sterilization Products, Inc. has received 5 total clearances in our database.
Advanced Sterilization Products, Inc. has 5 FDA actions in our database, including 5 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 Advanced Sterilization Products, Inc. have FDA actions?
Advanced Sterilization Products, Inc. has 5 FDA actions in our database, including 0 recalls and 5 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "K252843" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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