Innovative Medical Technologies, Inc.: FDA filings under this applicant name
FDA lists 6 510(k) clearances under the applicant name “Innovative Medical Technologies, Inc.” (first 1986, latest 2023), across 5 product codes in 4 review panels. Median 510(k) review time under this name: 239 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 | 1 | 244 |
| 2014 | 0 | — |
| 2015 | 0 | — |
| 2016 | 0 | — |
| 2017 | 0 | — |
| 2018 | 0 | — |
| 2019 | 0 | — |
| 2020 | 0 | — |
| 2021 | 0 | — |
| 2022 | 0 | — |
| 2023 | 1 | 589 |
| 2024 | 0 | — |
| 2025 | 0 | — |
| 2026 | 0 | — |
Review time against the same product codes
Since 2017, 510(k)s cleared under the name Innovative Medical Technologies, Inc. took a median 589 days from FDA receipt to decision. All cleared 510(k)s in the same product codes over the same years took a median 124 days.
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| JKA | Tubes, Vials, Systems, Serum Separators, Blood Collection | 2 | 2 |
| FPP | Stretcher, Hand-Carried | 1 | 1 |
| GIO | Tube, Collection, Capillary Blood | 1 | 1 |
| KPR | System, X-Ray, Stationary | 1 | 1 |
Plus 1 more product codes.
Review panels
- Clinical Chemistry (2)
- Hematology (1)
- General Hospital (1)
- Radiology (1)
Most recent Innovative Medical Technologies, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K220458 | UltraFlo-R Push Button Blood Collection Set | JKA | 2023-09-29 | 589 |
| K123987 | IMPROVE BLOOD COLLECTION SET AND IMPROSAFE BLOOD COLLECTION SET | JKA | 2013-08-27 | 244 |
| K972969 | QUICK-DRAW CAPILLARY WHOLE BLOOD COLLECTION SYSTEM | GIO | 1997-09-22 | 42 |
| K936087 | CARPAL BOX | KPR | 1994-10-20 | 303 |
| K904237 | RAPID IMMOBILIZATION DEVICE OR R.I.D. SYSTEM | FPP | 1991-05-09 | 234 |
| K854194 | IMT ULTRASONIC STRIDE MONITOR | — | 1986-05-02 | 199 |
Recalls
openFDA lists no recalls under a recalling firm named Innovative Medical Technologies, 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.
- Innovative Health, LLC (48 510(k)s)
- Innovative Medical Systems, Inc. (22 510(k)s)
- Innovative Technologies , Ltd. (14 510(k)s)
- Innovative Surgical Products, Inc. (12 510(k)s)
- Innovative Diagnostic Systems, Inc. (11 510(k)s)
- Innovative Gloves Co;, Ltd. (9 510(k)s)
- Innovative Surgical Designs, Inc. (9 510(k)s)
- Innovative Bioceramix, Inc. (8 510(k)s)
- Innovative Surgical, Inc. (7 510(k)s)
- Innovative Spinal Technologies, Inc. (4 510(k)s)
- Innovative Therapies, Inc. (4 510(k)s)
- Innovative Trauma Care, Inc. (4 510(k)s)
Frequently asked questions
How many FDA 510(k) clearances are listed under Innovative Medical Technologies, Inc.?
FDA lists 6 510(k) clearances under the applicant name “Innovative Medical Technologies, Inc.” (first 1986, latest 2023), across 5 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 Innovative Medical Technologies, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Innovative Medical Technologies, Inc. is 239 days.
Which FDA product codes appear under Innovative Medical Technologies, Inc.?
The most frequent FDA product codes under this applicant name are JKA (Tubes, Vials, Systems, Serum Separators, Blood Collection, 2); FPP (Stretcher, Hand-Carried, 1); GIO (Tube, Collection, Capillary Blood, 1).
Next steps
- See all 6 Innovative Medical Technologies, Inc. clearances with predicates and recalls
- Run predicate analysis for product code JKA, Innovative Medical Technologies, 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.