Instranetics, Inc.: FDA filings under this applicant name
FDA lists 10 510(k) clearances under the applicant name “Instranetics, Inc.” (first 1977, latest 1983), across 6 product codes in 4 review panels. Median 510(k) review time under this name: 22 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 |
|---|---|---|---|
| KDC | Instrument, Surgical, Disposable | 5 | 5 |
| FPA | Set, Administration, Intravascular | 1 | 1 |
| FSM | Tray, Surgical, Instrument | 1 | 1 |
| HBA | Neurosurgical Paddie | 1 | 1 |
| HXB | Probe | 1 | 1 |
| MMK | Container, Sharps | 1 | 1 |
Review panels
- General and Plastic Surgery (6)
- General Hospital (2)
- Neurology (1)
- Orthopedic (1)
Most recent Instranetics, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K823430 | INSTRA-SAFE | FSM | 1983-01-07 | 52 |
| K811824 | CAUTERY CADDY PAD | KDC | 1981-07-20 | 21 |
| K811823 | SHARPS CADDY FB | KDC | 1981-07-20 | 21 |
| K811822 | TIP-VU | KDC | 1981-07-20 | 21 |
| K810294 | LINE CADDY | HXB | 1981-02-26 | 22 |
| K810208 | BLADE SAFE | MMK | 1981-02-12 | 17 |
| K802865 | SAFE T COUNT | KDC | 1980-12-18 | 36 |
| K802866 | SHARPS CADDY MAGNETIC & SHARPS CADDY FOA | KDC | 1980-11-17 | 5 |
| K781575 | DISPOSABLE LYMPHANGIOGRAM SET | FPA | 1978-12-04 | 81 |
| K770894 | NEURO-SORB PATTIES | HBA | 1977-06-20 | 35 |
Recalls
openFDA lists no recalls under a recalling firm named Instranetics, 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 Instranetics, Inc.?
FDA lists 10 510(k) clearances under the applicant name “Instranetics, Inc.” (first 1977, latest 1983), across 6 product codes in 4 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 Instranetics, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Instranetics, Inc. is 22 days.
Which FDA product codes appear under Instranetics, Inc.?
The most frequent FDA product codes under this applicant name are KDC (Instrument, Surgical, Disposable, 5); FPA (Set, Administration, Intravascular, 1); FSM (Tray, Surgical, Instrument, 1).
Next steps
- See all 10 Instranetics, Inc. clearances with predicates and recalls
- Run predicate analysis for product code KDC, Instranetics, 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.