# Clarus Medical Systems, Inc.

- Location (FDA's records): Minneapolis, MN
- FDA decisions: 22 (1992–1998): 22 510(k) clearances
- Product codes: GWG (7), HRX (4), OCV (1), GBZ (1), HLX (1), FTI (1), GEX (1), GAD (1), LYK (1), ERA (1), EOB (1), FHO (1)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 9 (1 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Medical Laser, Inc.: 1 (https://510kreport.com/company/medical-laser)
- Smith & Nephew Richards, Inc.: 1 (https://510kreport.com/company/smith-nephew-richards)

## Firms that cite its devices most
- Clarus Medical, LLC: 6 (https://510kreport.com/company/clarus-medical)
- Omnisonics Medical Technologies: 1 (https://510kreport.com/company/omnisonics-medical-technologies)
- Richard Wolf Medical Instruments Corp.: 1 (https://510kreport.com/company/richard-wolf-medical-instruments)

## Its most-cited devices
- K922881: Clarus Models 1100, 1101, 1102, 1103 Laser Disc (1992), cited by 3
- K962255: Clarus Murphypen Endoscope (2127-XXX) (1996), cited by 2
- K941188: Clarus Neuro Endoscope  (Model 2230) (1995), cited by 1
- K945633: Neuro Channel Endoscope Model 2232 (1995), cited by 1
- K971455: Clarus Model 5197 Sightlite (1997), cited by 1
- K974579: Percscope Model 2600 (1998), cited by 1

## Recent decisions
- K980588: Clarus Endoscopic Discectomy System Sitetrac Model 6000 (Aug 18, 1998)
- K974579: Percscope Model 2600 (Feb 18, 1998)
- K971584: Clarus Model 2127-900 Series Endoscope Adater (2127-900 Series) (May 23, 1997)
- K971455: Clarus Model 5197 Sightlite (May 20, 1997)
- K960915: Clarus Neuropen Endoscopic Placement Kit Model 2125-XXX (Dec 24, 1996)
- K962255: Clarus Murphypen Endoscope (2127-XXX) (Sep 11, 1996)
- K955598: Clarus Spinepen Model 2126 (Feb 6, 1996)
- K953685: Instrument Scope (Oct 12, 1995)

Source page: https://510kreport.com/company/clarus-medical-systems