Neuro Technology: FDA filings under this applicant name
FDA lists 5 510(k) clearances under the applicant name “Neuro Technology” (first 1982, latest 1993), across 3 product codes in 1 review panel. Median 510(k) review time under this name: 199 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 |
|---|---|---|---|
| BSP | Needle, Conduction, Anesthetic (W/Wo Introducer) | 2 | 2 |
| BXN | Stimulator, Nerve, Battery-Powered | 2 | 2 |
| CAZ | Anesthesia Conduction Kit | 1 | 1 |
Review panels
- Anesthesiology (5)
Most recent Neuro Technology 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K925014 | E-SP COMBINED EPI SPINAL MINISET | CAZ | 1993-04-19 | 199 |
| K901810 | MICRO-SP LUMBAR PUNCTURE (SPINAL) NEEDLE | BSP | 1991-05-30 | 405 |
| K901811 | ADD'L DATA E-SP MULTIPURPOSE EPIDURAL SPINALNEEDLE | BSP | 1991-05-28 | 403 |
| K822139 | STIMPEN | BXN | 1982-09-13 | 56 |
| K822138 | NEUROSTIM II | BXN | 1982-07-30 | 11 |
Recalls
openFDA lists no recalls under a recalling firm named Neuro Technology.
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.
- Neuro Navigational Corp. (23 510(k)s)
- Neuro Supplies, Inc. (5 510(k)s)
- Neuro Kinetics, Inc. (4 510(k)s)
- Neuro Resource Group, Inc. (4 510(k)s)
- Neuro Scan Labs (3 510(k)s)
- Neuro Therm, Inc. (3 510(k)s)
- Neuro Vasx, Inc. (2 510(k)s)
- Neuro Diagnostic Devices (1 510(k)s)
- Neuro Event Labs OY (1 510(k)s)
- Neuro Spinal Innovation, Inc. (1 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Neuro Technology?
FDA lists 5 510(k) clearances under the applicant name “Neuro Technology” (first 1982, latest 1993), across 3 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 Neuro Technology?
The median time from FDA receipt to decision across 510(k)s cleared under the name Neuro Technology is 199 days.
Which FDA product codes appear under Neuro Technology?
The most frequent FDA product codes under this applicant name are BSP (Needle, Conduction, Anesthetic (W/Wo Introducer), 2); BXN (Stimulator, Nerve, Battery-Powered, 2); CAZ (Anesthesia Conduction Kit, 1).
Next steps
- See all 5 Neuro Technology clearances with predicates and recalls
- Run predicate analysis for product code BSP, Neuro Technology'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.