Wright Linear Pump, Inc.: FDA filings under this applicant name
FDA lists 6 510(k) clearances under the applicant name “Wright Linear Pump, Inc.” (first 1983, latest 2007), across 2 product codes in 2 review panels. Median 510(k) review time under this name: 148 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 |
|---|---|---|---|
| JOW | Sleeve, Limb, Compressible | 5 | 5 |
| DWL | Stocking, Medical Support (To Prevent Pooling Of Blood In Legs) | 1 | 1 |
Review panels
- Cardiovascular (5)
- General Hospital (1)
Most recent Wright Linear Pump, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K071040 | WRIGHT MODEL 51 AND 52 SEQUENTIAL COMPRESSION SYSTEMS | JOW | 2007-05-22 | 40 |
| K961891 | WLP SINGLE-SEGMENT VERSION WLP SOLO VII | JOW | 1996-11-06 | 181 |
| K961797 | WLP GRADIENT SEQUENTIAL VERSION/WLP PROLITE/WLP WLP-II LITE | JOW | 1996-11-06 | 181 |
| K961292 | WLP SEQUENTIAL VERSION MODEL WLP SOLO VI, WLP SOLO SEQUENTIAL | JOW | 1996-11-06 | 216 |
| K883186 | WRIGHT GRADIENT PRESSURE SUPPORT STOCKINGS | DWL | 1988-11-21 | 116 |
| K830577 | LINEAR PUMP #4370975 | JOW | 1983-05-25 | 91 |
Recalls
openFDA lists no recalls under a recalling firm named Wright Linear Pump, 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.
- Wright Medical (6 510(k)s)
- Wright Medical Technology, Inc. (Stryker) (3 510(k)s)
- Wright Medical Technology, Inc. (Stryker Corporation) (2 510(k)s)
- Wright Health Group , Ltd. (1 510(k)s)
- Wright Industries (1 510(k)s)
- Wright Laboratories, Inc. (1 510(k)s)
- Wright Medical Technology (1 510(k)s)
- Wright Therapy Products, Inc. (1 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Wright Linear Pump, Inc.?
FDA lists 6 510(k) clearances under the applicant name “Wright Linear Pump, Inc.” (first 1983, latest 2007), 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 Wright Linear Pump, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Wright Linear Pump, Inc. is 148 days.
Which FDA product codes appear under Wright Linear Pump, Inc.?
The most frequent FDA product codes under this applicant name are JOW (Sleeve, Limb, Compressible, 5); DWL (Stocking, Medical Support (To Prevent Pooling Of Blood In Legs), 1).
Next steps
- See all 6 Wright Linear Pump, Inc. clearances with predicates and recalls
- Run predicate analysis for product code JOW, Wright Linear Pump, 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.