Cleared Special

K263530 - V-Pro maX 2 Low Temperature Sterilization System

K263530 is an FDA 510(k) clearance for V-Pro maX 2 Low Temperature Sterilizati..., manufactured by Steris. The device is a Class 2 General Hospital device with product code MLR cleared through the Special 510(k) pathway after a 30-day FDA review.

K263530 · Steris · General Hospital
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Oct 2026
Decision
30d
Days
Class 2
Risk

K263530 is an FDA 510(k) clearance for the V-Pro maX 2 Low Temperature Sterilization System. Classified as Sterilizer, Chemical (product code MLR), Class II - Special Controls.

Submitted by Steris (Mentor, US). The FDA issued a Cleared decision on October 29, 2026 after a review of 30 days - a notably fast clearance cycle.

This device falls under the General Hospital FDA review panel, regulated under 21 CFR 880.6860 - the FDA general hospital device framework. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Low regulatory complexity profile. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

FDA 510(k) Submission Details - K263530

510(k) Number K263530 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 29, 2026
Decision Date October 29, 2026
Days to Decision 30 days
Submission Type Special
Review Panel General Hospital (HO)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
99d faster than avg
Panel avg: 129d · This submission: 30d
Pathway characteristics
Modification to existing cleared device.

MLR Device Classification - Class 2, Special Controls

Product Code MLR Sterilizer, Chemical
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 880.6860
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most General Hospital devices follow this clearance model.

Regulatory Peers - MLR Sterilizer, Chemical

All 47
Devices cleared under the same product code (MLR) and FDA review panel - the closest regulatory comparables to K263530.
STERRAD 100NX Sterilization System with ALLClear Technology (10104)
K252843 · Advanced Sterilization Products, Inc. · Apr 2026
STERRAD® 100NX Sterilizer with ALLClear™ Technology (10104)
K250802 · Advanced Sterilization Products, Inc. · Apr 2025
LOWTEM Crystal 120
K231893 · Lowtem Co., Ltd. · Sep 2024
STERRAD® 100NX Sterilizer with ALLClear™ Technology and ULTRA GI™ Cycle (10104)
K234082 · Advanced Sterilization Products · Jul 2024
SteroScope® Sterilization Technology System
K233762 · Ideate Medical, Inc. · Jun 2024
V-PRO maX 2 Low Temperature Sterilization System
K233065 · Steris · Oct 2023
K263530 · V-Pro maX 2 Low Temperature Sterilization System
Download PDF FDA Summary Steris