Mednet Locator, Inc.: FDA filings under this applicant name
FDA lists 9 510(k) clearances under the applicant name “Mednet Locator, Inc.” (first 1997, latest 2000), across 4 product codes in 1 review panel. Median 510(k) review time under this name: 54 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 |
|---|---|---|---|
| ETA | Replacement, Ossicular Prosthesis, Total | 3 | 3 |
| ETD | Tube, Tympanostomy | 3 | 3 |
| ETB | Prosthesis, Partial Ossicular Replacement | 2 | 2 |
| ERL | Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece | 1 | 1 |
Review panels
Most recent Mednet Locator, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K001406 | HA/GOLD TOTAL AND PARTIAL, REGULAR AND OFFSET, OSSICULAR REPLACEMENT PROSTHESES | ETA | 2000-08-08 | 97 |
| K001404 | GOLD TOTAL AND PARTIAL, REGULAR AND OFFSET, OSSICULAR REPLACEMENT PROSTHESES, GOLD TOTAL WITH FOUNTIAN HEAD, GOLD PISTON | ETA | 2000-08-08 | 97 |
| K974174 | ULTRABUR | ERL | 1998-03-10 | 124 |
| K972737 | CAUSSE PISTON | ETB | 1997-09-05 | 45 |
| K972735 | TOTAL OSSICULAR REPLACEMENT PROSTHESIS (TORP) | ETA | 1997-09-05 | 45 |
| K972734 | PARTIAL OSSICULAR REPLACEMENT PROSTHESIS (PORP) | ETB | 1997-09-05 | 45 |
| K972126 | MYRINGOTOMY TUBE | ETD | 1997-07-29 | 54 |
| K972400 | MYRINGOTOMY TUBE - BOBBIN WITH TAB | ETD | 1997-07-23 | 48 |
| K971943 | MYRINGOTOMY TUBE | ETD | 1997-07-23 | 57 |
Recalls
openFDA lists no recalls under a recalling firm named Mednet Locator, 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.
Other FDA applicant names starting with the same word
FDA records these as separate applicants. Some may belong to the same corporate group and some may not; their filings are not included in the counts above.
- Mednet, Inc. (12 510(k)s)
- Mednet Services, Inc. (2 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Mednet Locator, Inc.?
FDA lists 9 510(k) clearances under the applicant name “Mednet Locator, Inc.” (first 1997, latest 2000), across 4 product codes 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 Mednet Locator, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Mednet Locator, Inc. is 54 days.
Which FDA product codes appear under Mednet Locator, Inc.?
The most frequent FDA product codes under this applicant name are ETA (Replacement, Ossicular Prosthesis, Total, 3); ETD (Tube, Tympanostomy, 3); ETB (Prosthesis, Partial Ossicular Replacement, 2).
Next steps
- See all 9 Mednet Locator, Inc. clearances with predicates and recalls
- Run predicate analysis for product code ETA, Mednet Locator, 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 (spelling variants such as punctuation and legal suffixes combined); filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.