Rln Systems, Inc.: FDA filings under this applicant name
FDA lists 5 510(k) clearances under the applicant name “Rln Systems, Inc.” (first 1989, latest 2001), across 1 product code in 1 review panel. Median 510(k) review time under this name: 79 days. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.
510(k) clearances per year
| Year | Clearances | Median review days |
|---|---|---|
| 2012 | 0 | — |
| 2013 | 0 | — |
| 2014 | 0 | — |
| 2015 | 0 | — |
| 2016 | 0 | — |
| 2017 | 0 | — |
| 2018 | 0 | — |
| 2019 | 0 | — |
| 2020 | 0 | — |
| 2021 | 0 | — |
| 2022 | 0 | — |
| 2023 | 0 | — |
| 2024 | 0 | — |
| 2025 | 0 | — |
| 2026 | 0 | — |
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| ETN | Stimulator, Nerve | 5 | 5 |
Review panels
Most recent Rln Systems, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K003745 | LARYNGEAL SURFACE ELECTRODE-ENDOTRACHEAL TUBE, M-500-ET, LSE-ET | ETN | 2001-01-16 | 43 |
| K954601 | NERVE LOCATOR/MONITOR SYSTEM MODIFICATION | ETN | 1995-12-22 | 101 |
| K925008 | RLN NERVE LOCATOR/MONITOR; MODEL A | ETN | 1992-11-24 | 53 |
| K912508 | NERVE LOCATOR/MONITOR SYSTEM, MODIFICATION | ETN | 1992-09-30 | 482 |
| K895676 | HEMOSTAT/STIMULATOR PROBE | ETN | 1989-12-08 | 79 |
Recalls
openFDA lists no recalls under a recalling firm named Rln Systems, Inc..
Recalling firms are matched to this applicant name by name only (same normalization), so related entities that recall under another name are not counted. A recall count says nothing about how safe one company's devices are compared with another's.
Frequently asked questions
How many FDA 510(k) clearances are listed under Rln Systems, Inc.?
FDA lists 5 510(k) clearances under the applicant name “Rln Systems, Inc.” (first 1989, latest 2001), across 1 product code in 1 review panel. Filings under other applicant names, such as subsidiaries, are not included.
How long has FDA taken to clear 510(k)s filed by Rln Systems, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Rln Systems, Inc. is 79 days.
Which FDA product codes appear under Rln Systems, Inc.?
The most frequent FDA product codes under this applicant name are ETN (Stimulator, Nerve, 5).
Next steps
- See all 5 Rln Systems, Inc. clearances with predicates and recalls
- Run predicate analysis for product code ETN, Rln Systems, Inc.'s most frequent
Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Each page covers one FDA applicant name, with punctuation and legal suffixes removed; filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.