Cooltouch Corp.: FDA filings under this applicant name
FDA lists 6 510(k) clearances under the applicant name “Cooltouch Corp.” (first 2000, latest 2006), across 1 product code in 1 review panel. Median 510(k) review time under this name: 90 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 |
|---|---|---|---|
| GEX | Powered Laser Surgical Instrument | 6 | 6 |
Review panels
Most recent Cooltouch Corp. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K060966 | COOLTOUCH VARIA ND:YAG LASER SYSTEM | GEX | 2006-07-31 | 115 |
| K040921 | COOLTOUCH, MODEL NS 160 | GEX | 2004-09-28 | 173 |
| K014035 | COOLTOUCH AND COOLTOUCH-II ND:YAG LASER SYSTEMS | GEX | 2002-03-07 | 90 |
| K010316 | COOLTOUCH VARIA ND:YAG LASER SYSTEM; COOLTOUCH VARIA-II ND:YAG LASER SYSTEM | GEX | 2001-05-01 | 88 |
| K003715 | COOLTOUCH ND:YAG LASER SYSTEM, COOLTOUCH-II ND:YAG LASER SYSTEM, MODEL COOLTOUCH, COOLTOUCH II | GEX | 2001-03-01 | 90 |
| K003781 | COOLTOUCH VARIA-II ND:YAG LASER SYSTEM | GEX | 2000-12-20 | 13 |
Recalls
openFDA lists no recalls under a recalling firm named Cooltouch Corp..
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 Cooltouch Corp.?
FDA lists 6 510(k) clearances under the applicant name “Cooltouch Corp.” (first 2000, latest 2006), across 1 product code 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 Cooltouch Corp.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Cooltouch Corp. is 90 days.
Which FDA product codes appear under Cooltouch Corp.?
The most frequent FDA product codes under this applicant name are GEX (Powered Laser Surgical Instrument, 6).
Next steps
- See all 6 Cooltouch Corp. clearances with predicates and recalls
- Run predicate analysis for product code GEX, Cooltouch Corp.'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.