Versius Monopolar Hook

Catalogue number 10420, listed by CMR Surgical Limited, United Kingdom, under Modular Electromechanical Surgical System. 1 manufacturer in China is registered for this product code.

Registry build 21.09.26
1manufacturer
1catalogue number
2510(k) clearances naming this product code
1recall

Who Else Makes It

Registered in Guangdong. One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code SCV
Manufacturer City Province Registered as Device types
Amphenol Alden Products Company Shenzhen Guangdong Contract manufacturer 24

Record

Regulatory record for Versius Monopolar Hook
Listed by CMR Surgical Limited, United Kingdom
FDA product code SCV
Device type Modular Electromechanical Surgical System
Device class Class 2
Regulation 21 CFR 878.4964
Establishment Specification developer, Manufacturer
510(k) K252111
Record published 2026-03-09

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Ethylene Oxide
Label carries lot or batch number, manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for Versius Monopolar Hook
Catalogue number Size Status
10420 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Hugo RAS Covidien LP 29
Versius Monopolar Bedside Unit Cable CMR Surgical Limited 1
Versius Bedside Unit Cable (Short) CMR Surgical Limited 1
Versius Instrument Bedside Unit CMR Surgical Limited 1
Versius Insulating Sleeve Accessory → Carton Pack (Qty 12 x 10021), 10022 CMR Surgical Limited 1
Versius Insulating Sleeve Accessory Shipper Pack (Quantity 8 x 10022 in a shippe CMR Surgical Limited 1
Versius Surgeon Console CMR Surgical Limited 1
Versius Bipolar Bedside Unit Cable CMR Surgical Limited 1
Versius Bipolar Fenestrated Grasper CMR Surgical Limited 1
Versius Endoscope 0° (vLimeLite) CMR Surgical Limited 1
Versius Camera Head (compatible with vLimeLite) CMR Surgical Limited 1
Versius Fenestrated Grasper CMR Surgical Limited 1

Showing 12 of 24. All products under Modular Electromechanical Surgical System

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K252111 2025-12-16
DEN230078 2024-10-11

Recalls Naming This Product

1 recall names this product by its own identifier, the 510(k) it is cleared under.

Recalls naming the identifiers of Versius Monopolar Hook
Recalled by Identified by Initiated FDA class Root cause Reason Quantity
CMR Surgical Limited 510(k) number 2026-06-09 Class II Software design (manufacturing process) Secure Boot was mistakenly not enabled at manufacturing time, which presents a potential cybersecurity risk. 2

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer