Rln Systems, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Rln Systems, Inc. makes
Rln Systems, Inc. makes medical devices such as hemostat/stimulator probes, nerve locator/monitor systems, and laryngeal surface electrode-endotracheal tubes. These products are used for various medical applications, including monitoring and stimulation. The company's devices include specific models like the M-500-ET and LSE-ET.
The company's portfolio is regulated as Class II devices and is listed in the FDA 510(k) registry. Rln Systems, Inc. is based in the US.
Catalogue
Hemostat/Stimulator Probe Ref K895676
Regimes: 510(k) Registry: 510(k)Nerve Locator/Monitor System, Modification Ref K912508
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Rln Nerve Locator/Monitor; Model A Ref K925008
Regimes: 510(k) Registry: 510(k)Nerve Locator/Monitor System Modification Ref K954601
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rln Systems, Inc. have in the registry?
The registry currently lists 5 devices for Rln Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rln Systems, Inc.'s devices?
Among its 5 most recently registered devices, Rln Systems, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Rln Systems, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Rln Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Rln Systems, Inc. in the registry?
The most recently registered devices listed for Rln Systems, Inc. include HEMOSTAT/STIMULATOR PROBE, NERVE LOCATOR/MONITOR SYSTEM, MODIFICATION, LARYNGEAL SURFACE ELECTRODE-ENDOTRACHEAL TUBE, M-500-ET, LSE-ET and RLN NERVE LOCATOR/MONITOR; MODEL A.