Cleared Traditional

K173085 - invendoscopy E210 System

K173085 is an FDA 510(k) clearance for invendoscopy E210 System, manufactured by Invendo Medical GmbH. The device is a Class 2 Gastroenterology & Urology device with product code FDF cleared through the Traditional 510(k) pathway after a 101-day FDA review.

K173085 · Invendo Medical GmbH · Gastroenterology & Urology device
Download Printable Device Report (PDF) Official FDA 510(k) Summary (PDF)
Optimized for regulatory review, auditing and printing
Jan 2018
Decision
101d
Days
Class 2
Risk

K173085 is an FDA 510(k) clearance for the invendoscopy E210 System. Classified as Colonoscope And Accessories, Flexible/rigid (product code FDF), Class II - Special Controls.

Submitted by Invendo Medical GmbH (Kissing, DE). The FDA issued a Cleared decision on January 8, 2018 after a review of 101 days - within the typical 510(k) review window.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.1500 - the FDA gastroenterology and urology device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Gastroenterology & Urology review framework, consistent with the majority of Class II 510(k) submissions.

FDA 510(k) Submission Details - K173085

510(k) Number K173085 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 29, 2017
Decision Date January 08, 2018
Days to Decision 101 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
30d faster than avg
Panel avg: 131d · This submission: 101d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FDF Device Classification - Class 2, Special Controls

Product Code FDF Colonoscope And Accessories, Flexible/rigid
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.1500
Definition To Examine Or Perform Procedures In The Colon Or Rectum For Reusable, Flexible Endoscopes In This Product Code, Validated Reprocessing Instructions And Reprocessing Validation Data Must Be Included In A 510(k) Submission (82 Fr 26807, Available At Https://www.gpo.gov/fdsys/pkg/fr-2017-06-09/pdf/2017-12007.pdf).
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 Gastroenterology & Urology devices follow this clearance model.

Regulatory Peers - FDF Colonoscope And Accessories, Flexible/rigid

All 112
Devices cleared under the same product code (FDF) and FDA review panel - the closest regulatory comparables to K173085.
DiLumen C2
K173317 · Lumendi, LLC · Apr 2018
FUJIFILM Endoscope Models EC-600HL and EC-600LS
K180405 · Fujifilm Corporation · Mar 2018
Focus Cap
K171673 · Gce Medical Corporation · Jan 2018
Pure-Vu System
K173392 · Motus GI Medical Technologies , Ltd. · Dec 2017
Medrobotics Flex Robotic System
K172036 · Medrobotics Corporation · Aug 2017
Flex Robotic System and Flex Colorectal Drive
K162330 · Medrobotics Corporation · May 2017