Data / Medical devices / United States / Innovative Innovations Inc.
Innovative Innovations Inc.: FDA-registered device maker in Henderson, NV, United States, 4 510(k) clearances
Innovative Innovations Inc. is registered with the FDA (registration 3005536872) in Henderson, NV, United States. It lists 11 device types. The FDA files 4 510(k) clearances under its listings, the newest dated June 20, 2005. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3005536872
- Address
- 1132 Santa Ynez Ave., Henderson, NV, United States, 89002
- Owner or operator
- INNOVATIVE INNOVATIO (9081220)
- Roles
- Repackager or relabeler
- First device listed
- April 17, 2007
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Blood Pressure Cuff | DXQ | 2 | Repackager or relabeler | accessdata.fda.gov |
| Continuous Measurement Thermometer | FLL | 2 | Repackager or relabeler | accessdata.fda.gov |
| Elevator, Ent | KAD | 1 | Repackager or relabeler | accessdata.fda.gov |
| Gouge, Nasal, Ent | KAQ | 1 | Repackager or relabeler | accessdata.fda.gov |
| Laryngoscope, Rigid | CCW | 1 | Repackager or relabeler | accessdata.fda.gov |
| Ophthalmoscope, Battery-Powered | HLJ | 2 | Repackager or relabeler | accessdata.fda.gov |
| Otoscope | ERA | 1 | Repackager or relabeler | accessdata.fda.gov |
| Scissors, General, Surgical | LRW | 1 | Repackager or relabeler | accessdata.fda.gov |
| Speculum, Ent | EPY | 1 | Repackager or relabeler | accessdata.fda.gov |
| Stethoscope, Manual | LDE | 1 | Repackager or relabeler | accessdata.fda.gov |
| System, Measurement, Blood-Pressure, Non-Invasive | DXN | 2 | Repackager or relabeler | 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 |
|---|---|---|---|---|---|---|
| June 20, 2005 | K051021 | ANEROID SPHYGMANOMETER WITH STETHOSCOPE, MODEL HS-50A | DXQ | Substantially Equivalent | Shanghai Lord International Trade Co., Ltd. | accessdata.fda.gov |
| December 2, 2004 | K041693 | WRIST DIGITAL BLOOD PRESSURE MONITOR (DIGITAL SPHYGMOMANOMETER), MW-300 SERIES | DXN | Substantially Equivalent | Hangzhou Hua'An Medical & Health Instruments Co., | accessdata.fda.gov |
| September 13, 2004 | K041694 | DIGITAL FLEXIBLE THERMOMETER, BASIC DIGITAL THERMOMETER, DITITAL PACIFIER THERMOMETER | FLL | Substantially Equivalent | Hangzhou Hua'An Medical & Health Instruments Co., | accessdata.fda.gov |
| September 13, 2004 | K041692 | INFRARED EAR THERMOMETER, ET-100 SERIES | FLL | Substantially Equivalent | Hangzhou Hua'An Medical & Health Instruments Co., | accessdata.fda.gov |
Compare with other makers
- All makers of Otoscope
- All makers of Gouge, Nasal, Ent
- All makers of Scissors, General, Surgical
- All makers of Continuous Measurement Thermometer
- All makers of Stethoscope, Manual
- All makers of System, Measurement, Blood-Pressure, Non-Invasive
Updated June 20, 2005. 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.