Omnitech Systems, Inc.: FDA filings under this applicant name
FDA lists 6 510(k) clearances under the applicant name “Omnitech Systems, Inc.” (first 1997, latest 2016), across 2 product codes in 2 review panels. Median 510(k) review time under this name: 92 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 | 1 | 347 |
| 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 |
|---|---|---|---|
| FAS | Electrode, Electrosurgical, Active, Urological | 4 | 4 |
| KNF | Coagulator-Cutter, Endoscopic, Unipolar (And Accessories) | 2 | 2 |
Review panels
Most recent Omnitech Systems, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K151976 | Omnitech HF Resection Electrodes, Omnitech HF Vaporization Electrode | FAS | 2016-06-27 | 347 |
| K050454 | OMNITECH FULGURATING ELECTRODE | FAS | 2005-05-27 | 94 |
| K981463 | OMNITECH RESECTOSCOPE ROLLER ELECTRODE | KNF | 1998-07-17 | 85 |
| K981464 | OMNITECH RESECTOSCOPE CUTTING LOOP ELECTRODE | KNF | 1998-07-10 | 78 |
| K964365 | RESECTOSCOPE CUTTING LOOP ELECTRODE | FAS | 1997-04-22 | 172 |
| K965093 | OMNITECH RESECTOSCOPE ROLLER ELECTRODE | FAS | 1997-03-19 | 90 |
Recalls
openFDA lists no recalls under a recalling firm named Omnitech 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 Omnitech Systems, Inc.?
FDA lists 6 510(k) clearances under the applicant name “Omnitech Systems, Inc.” (first 1997, latest 2016), across 2 product codes in 2 review panels. Filings under other applicant names, such as subsidiaries, are not included.
How long has FDA taken to clear 510(k)s filed by Omnitech Systems, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Omnitech Systems, Inc. is 92 days.
Which FDA product codes appear under Omnitech Systems, Inc.?
The most frequent FDA product codes under this applicant name are FAS (Electrode, Electrosurgical, Active, Urological, 4); KNF (Coagulator-Cutter, Endoscopic, Unipolar (And Accessories), 2).
Next steps
- See all 6 Omnitech Systems, Inc. clearances with predicates and recalls
- Run predicate analysis for product code FAS, Omnitech 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.