510(k) Report

510(k) · Cleared

Cleared

V-PRO maX 2 Low Temperature Sterilization System

K233065510(k) SpecialCleared Oct 20, 202324-day reviewClass II21 CFR 880.6860

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Steris · MLR Sterilizer, Chemical

Cleared on Oct 20, 2023 as substantially equivalent to K223476 (STERIS Corporation, 2023) after a 24-day review. Its family tree reaches back 3 generations to 2019.

Decided
Oct 20, 2023
Review
24 days
Class
Class II
Product code
MLR
Recalls
None
Predicates
1

Its longest line of descent runs back 3 generations to K190103 (2019). No later device cites it as a predicate yet.

  1. Root · 3 generations backK190103 V-PRO maX 2 Low Temperature Sterilization System, V-PRO maX Low…STERIS Corporation · 2019
  2. 2 generations backK222093 V-PRO maX 2 Low Temperature Sterilization System, V-PRO maX Low…Steris · 2022
  3. 1 generation backK223476 V-PRO maX 2 Low Temperature Sterilization SystemSTERIS Corporation · 2023
  4. This deviceK233065 V-PRO maX 2 Low Temperature Sterilization SystemSteris · 2023
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K190103V-PRO maX 2 Low Temperature Sterilization System, V-PRO maX Low Temperature…STERIS Corporation2019—
−2K222093V-PRO maX 2 Low Temperature Sterilization System, V-PRO maX Low Temperature…Steris2022—
−1K223476V-PRO maX 2 Low Temperature Sterilization SystemSTERIS Corporation2023—
0 (this device)K233065V-PRO maX 2 Low Temperature Sterilization SystemSteris2023—
FIG. 1 — Lineage of K233065, 2019–2023Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in MLR? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new MLR device

  1. #1 K250802 STERRAD® 100NX Sterilizer with ALLClear™…score 14.0 · 7 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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What was it cleared against? (1)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K223476V-PRO maX 2 Low Temperature Sterilization System
Summary page 7
…MLR 2. Predicate Device The claimed primary predicate device is the V-PRO maX 2 Low Temperature Sterilization Systems, cleared most recently under K223476. VAPROX HC Sterilant is the required sterilant used in the V-PRO Low Temperature Sterilization Systems. The comparison…
STERIS Corporation2023—

What descends from it?

No later submission names this one as a predicate yet.

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 4 years and passes through 2 companies; a new generation was cleared every 11 months on median.
  • None of the 3 ancestors has a recall.

How does its category compare?

All MLR devices

MLR Sterilizer, Chemical: FDA decisions, review times, recalls and adverse event reports over 20 years. 2023, this device’s year, is highlighted.

FDA decisions per year · MLR

1in 2025

2007: 22009: 12011: 62012: 22013: 12014: 22015: 12016: 42017: 22018: 22019: 42021: 22022: 22023: 52024: 32025: 12026 (partial year): 1
2007high 6 (2011) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MLR

216in 2024

2011: 214 days median2016: 183 days median2019: 90 days median2023: 222 days median2024: 216 days median
2007high 222 (2023) · low 90 (2019)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · MLR

1in 2017

2007: 52008: 82009: 22010: 12011: 22012: 32013: 92014: 32017: 1
2007high 9 (2013) · low 0 (2015)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · MLR

46in 2025

2007: 2722008: 5362009: 4332010: 2112011: 342012: 1012013: 5412014: 3992015: 4122016: 2862017: 2792018: 2892019: 2222020: 1742021: 2022022: 1882023: 1402024: 442025: 46
2007high 541 (2013) · low 34 (2011)2025

MAUDE reports naming product code MLR, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20072—5272
20080—8536
20091—2433
20100—1211
20116214234
20122—3101
20131—9541
20142—3399
20151—0412
201641830286
20172—1279
20182—0289
20194900222
20200—0174
20212—0202
20222—0188
202352220140
20243216044
20251—046
20261—0—

What is it indicated for?

The V-PRO maX 2 Low Temperature Sterilization System using VAPROX HC Sterilant is intended for use in the terminal sterilization of properly prepared (cleaned, rinsed and dried) medical devices in Healthcare Facilities. The preprogrammed sterilization cycles operate at low pressure and temperature, suitable for processing medical devices without leaving toxic residues. Each Cycle can sterilize non-lumened instruments with diffusion-restricted spaces such…

Read the full statement (767 words)

The V-PRO maX 2 Low Temperature Sterilization System using VAPROX HC Sterilant is intended for use in the terminal sterilization of properly prepared (cleaned, rinsed and dried) medical devices in Healthcare Facilities. The preprogrammed sterilization cycles operate at low pressure and temperature, suitable for processing medical devices without leaving toxic residues.

Each Cycle can sterilize non-lumened instruments with diffusion-restricted spaces such as the hinged portion of forceps and scissors.

The Non Lumen Cycle can sterilize: ‡

Non-lumened instruments including non-lumened general medical instruments, non-lumened rigid, semi-rigid and flexible endoscopes.

‡ The validation studies were conducted using a validation load consisting of two instrument trays for a total weight of 50 lbs (22.7 kg).

The Fast Non Lumen Cycle can sterilize: *

Non-lumened instruments including non-lumened general medical instruments, non-lumened rigid, semi-rigid and flexible endoscopes.

* The validation studies were conducted using a validation load consisting of one pouched instrument tray for a total weight of 11 lbs (5 kg).

The Flexible Cycle can sterilize:

Single or dual lumen surgical flexible endoscopes (such as those used in ENT, Urology and Surgical Care) and bronchoscopes in either of the two load configurations:

1. Two flexible endoscopes with a light cord (if not integral to endoscope) and mat with no additional load. * The flexible endoscopes may contain single or dual channel lumens that are ≥ 1 mm internal diameter (ID) and ≤ 1050 mm in length.

* The validation studies were conducted with two flexible endoscopes, each packaged into a tray with silicone mat and light cord (if not integral to endoscope).

2. One flexible endoscope with a light cord (if not integral to endoscope), endoscope accessories, mat, and additional instruments. †† The flexible endoscope may contain single or dual channel lumens that are ≥ 1 mm ID and ≤ 1050 mm in length

• Additional instruments may include non-lumened or lumened medical devices with the following configurations:

o Single, dual or triple channel stainless steel lumen that is

• ≥ 0.48 mm ID and ≤ 100 mm in length

†† The validation studies were conducted with a flexible endoscope in a tray with endoscope accessories, silicone mat, light cord (if not integral to endoscope) and 5 stainless steel lumens. Also included in the load was a tray with additional instruments, and silicone mat for a total weight of 24 lbs (11 kg).

The Lumen Cycle can sterilize: †

Medical devices with the following configurations:

• Single, dual or triple channeled stainless steel lumen that are:

• ≥ 0.77 mm ID and ≤ 527 mm in length

• ≥ 0.8 mm ID and ≤ 542 mm in length

• ≥ 0.48 mm ID and ≤ 100 mm in length

• Dead end lumen that is ≥ 1.3 mm ID and ≤ 73 mm in length

• Rigid non-metallic lumen (such as those used in endoscope sheaths, take-apart forceps and trocars) that are:

• ≥ 3 mm ID and ≤ 298 mm in length

• ≥ 4 mm ID and ≤ 424 mm in length

† Validation testing for all lumen sizes was conducted using a maximum of 20 lumens per load. Hospital loads should not exceed the maximum number of lumens validated by this testing. The validation studies were performed using a validation load consisting of two instrument trays and two pouches for a total weight of 19.65 lbs (8.9 kg).

The Specialty Cycle can sterilize:

Patient-specific surgical guides (e.g. osteotomy, shoulder, hip, knee, spine) or anatomical models fabricated via additive manufacturing (3D printing) processes and intended for single-use during operative procedures.*

or

Non-lumened instruments including non-lumened general medical instruments, non-lumened rigid, semi-rigid and flexible endoscopes.**

3D Printed Devices constructed of the following materials, and lumen if present, must be sterilized in the Specialty Cycle identified

Material Manufacturer Specialty Cycle Lumens

Surgical Guide Resin Formlabs F ≥3 mm ID x ≤30 mm L

BioMed Amber Resin Formlabs F ≥3 mm ID x ≤30 mm L

Dental LT Clear V2 Resin Formlabs D ≥3 mm ID x ≤30 mm L

BioMed Clear Resin Formlabs D ≥3 mm ID x ≤30 mm L

MED615RGD Stratasys E ≥3 mm ID x ≤20 mm L

MED620 Stratasys E ≥3 mm ID x ≤20 mm L

MED610 Stratasys E ≥3 mm ID x ≤20 mm L

* The validation studies were conducted using a validation load consisting of single-pouched guide(s)/model(s) (with or without tray) with a total weight of 5 lbs. (2.3 kg) of 3D printed material.

** The validation studies were conducted using a validation load consisting of pouched devices (with or without tray) for a total weight of 11 lbs. (5 kg).

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K233065: V-PRO maX 2 Low Temperature Sterilization System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K233065

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026