# Rln Systems, Inc.

- Location (FDA's records): Jefferson City, MO
- FDA decisions: 5 (1989–2001): 5 510(k) clearances
- Product codes: ETN (5)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 9 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Neurovision Medical Products, Inc.: 5 (https://510kreport.com/company/neurovision-medical-products)
- Medtronic Xomed, Inc.: 1 (https://510kreport.com/company/medtronic-xomed)
- Inomed Medizintechnik GmbH: 1 (https://510kreport.com/company/inomed-medizintechnik)
- Spes Medica Srl: 1 (https://510kreport.com/company/spes-medica)
- The Magstim Company, Ltd.: 1 (https://510kreport.com/company/magstim)

## Its most-cited devices
- K003745: Laryngeal Surface Electrode-Endotracheal Tube, M-500-ET, Lse-ET (2001), cited by 4
- K954601: Nerve Locator/Monitor System Modification (1995), cited by 3
- K895676: Hemostat/Stimulator Probe (1989), cited by 2

## Recent decisions
- K003745: Laryngeal Surface Electrode-Endotracheal Tube, M-500-ET, Lse-ET (Jan 16, 2001)
- K954601: Nerve Locator/Monitor System Modification (Dec 22, 1995)
- K925008: RLN Nerve Locator/Monitor; Model a (Nov 24, 1992)
- K912508: Nerve Locator/Monitor System, Modification (Sep 30, 1992)
- K895676: Hemostat/Stimulator Probe (Dec 8, 1989)

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