Data / Medical devices / United States / Innovative Medical Technologies, Inc
Innovative Medical Technologies, Inc: FDA-registered device maker in Overland Park, KS, United States, 3 510(k) clearances
Innovative Medical Technologies, Inc is registered with the FDA (registration 1933913) in Overland Park, KS, United States. It lists 4 device types. The FDA files 3 510(k) clearances under its listings, the newest dated September 29, 2023. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1933913
- FEI number
- 3001451226
- Address
- 16904 Rosehill St, Overland Park, KS, United States, 66221
- Owner or operator
- INNOVATIVE MEDICAL TECHNOLOGIES, INC. (9029704)
- Roles
- Complaint file establishment, Specification developer
- First device listed
- October 30, 1997
- Registered through
- 2026
- Brand names listed
- UltraFlo-A, UltraFlo-C, UltraFlo-L Safety Infusion and Blood Collection Set, UltraFlo-R Infusion and Blood Collection Set, UltraFlo-S Safety Infusion and Blood Collection Set, UltraFlo-T, UltraFlo-V
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Set, Administration, Intravascular | FPA | 2 | Specification developer | accessdata.fda.gov |
| System, Blood Collection, Vacuum-Assisted, Manual | KST | 1 | Complaint file establishment | accessdata.fda.gov |
| Tube, Collection, Capillary Blood | GIO | 1 | Complaint file establishment | accessdata.fda.gov |
| Tubes, Vials, Systems, Serum Separators, Blood Collection | JKA | 2 | Complaint file establishment, Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| September 29, 2023 | K220458 | UltraFlo-R Push Button Blood Collection Set | JKA | Substantially Equivalent | Innovative Medical Technologies, Inc. | accessdata.fda.gov |
| June 4, 2018 | K172763 | Blood Collecting Needle, Safety Blood Collecting Needle, Blood Collecting Needle with Holder, Safety Blood Collecting Needle with Holder, Blood Collecting Set, Safety Blood Collecting Set, Blood Collecting Set with Holder, Safety Blood Collecting Set with Holder | JKA | Substantially Equivalent | Zhejiang Kindly Medical Devices Co., Ltd. | accessdata.fda.gov |
| August 27, 2013 | K123987 | IMPROVE BLOOD COLLECTION SET AND IMPROSAFE BLOOD COLLECTION SET | JKA | Substantially Equivalent | Innovative Medical Technologies, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Tubes, Vials, Systems, Serum Separators, Blood Collection
- All makers of Set, Administration, Intravascular
- All makers of System, Blood Collection, Vacuum-Assisted, Manual
- All makers of Tube, Collection, Capillary Blood
Updated September 29, 2023. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.