Data / Medical devices / United States / International Medical Development, Inc.
International Medical Development, Inc.: FDA-registered device maker in Huntsville, UT, United States, 3 510(k) clearances
International Medical Development, Inc. is registered with the FDA (registration 1722686) in Huntsville, UT, United States. It lists 1 device type. The FDA files 3 510(k) clearances under its listings, the newest dated February 2, 2018. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1722686
- FEI number
- 1000220636
- Address
- 560 Hwy 39, Huntsville, UT, United States, 84317
- Owner or operator
- INTERNATIONAL MEDICAL DEVELOPMENT, INC. (9011668)
- Roles
- Repackager or relabeler, Specification developer
- First device listed
- December 2, 2008
- Registered through
- 2026
- Brand names listed
- International Medical Development, Lumbar Puncture Needle (And Mylogram; Pediatric)
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Needle, Conduction, Anesthetic (W/Wo Introducer) | BSP | 2 | Repackager or relabeler, 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 |
|---|---|---|---|---|---|---|
| February 2, 2018 | K170112 | IMD's Lumbar Puncture Needle | BSP | Substantially Equivalent | International Medical Development, Inc.(Imd) | accessdata.fda.gov |
| October 5, 2007 | K070354 | IMD'S ANESTHESIA NEEDLES (TUOHY, QUINCKE AND PENCIL POINT) | BSP | Substantially Equivalent | International Medical Development, Inc. | accessdata.fda.gov |
| September 22, 1993 | K931644 | GERTIE MARX NEEDLE | BSP | Substantially Equivalent | Intl. Medical-Dental Products USA, Inc. | accessdata.fda.gov |
Compare with other makers
Updated February 2, 2018. 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.