# K051827: Joimax Endoscope/Multiscope, Thessys Foraminoscope/Multiscope, Thessys Laminoscope/Multiscope

- Pathway: 510(k) (Traditional)
- Applicant: Joimax GmbH
- Decided: Aug 12, 2005 after 37 days
- Product code: HRX (Arthroscope)
- Device class: 2
- Regulation: 21 CFR 888.1100
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
76 later devices descend from it; 8 cite it directly.
0 of 77 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Richard Wolf Discoscope with Panoview Plus Optics: named in the summary without a submission number
- (no number) Richard Wolf YESS: named in the summary without a submission number
- (no number) Endius Spine Endoscope: named in the summary without a submission number
- (no number) Pollux Arthroscope: named in the summary without a submission number

## Most influential descendants
- K082355: Visionsense Stereoscopic Vision System (2008), 37 descendants of its own
- K141002: VS3 Stereoscopic High Definition Vision System (2014), 36 descendants of its own
- K152204: VS3-IR system (2015), 34 descendants of its own
- K162882: KARL STORZ ICG Imaging System (2017), 32 descendants of its own
- K171238: KARL STORZ ICG Imaging System (2017), 31 descendants of its own

## Indications for use
The THESSYS Multiscope is intended to visualize the inside of the patient through a cannulated incision for diagnostic and surgical procedures, such as arthroplasty, nucleotomy, discectomy, and foraminotomy.

Source page: https://510kreport.com/device/K051827
Methodology: https://510kreport.com/methodology