Data / Medical devices / United States / Metric Medical Devices, Inc.
Metric Medical Devices, Inc.: FDA-registered device maker in Helotes, TX, United States, 3 510(k) clearances
Metric Medical Devices, Inc. is registered with the FDA (registration 3009746186) in Helotes, TX, United States. It lists 3 device types. The FDA files 3 510(k) clearances under its listings, the newest dated May 29, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3009746186
- Address
- 846 Silver SPGS, Helotes, TX, United States, 78023
- Owner or operator
- Metric Medical Devices, Inc. (10043762)
- Roles
- Manufacturer, Specification developer
- First device listed
- March 19, 2013
- Registered through
- 2026
- Brand names listed
- IFS, Intramedullary Fixation Scaffold, LINK External Fixator, Super Staple¿ Classic
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component | KTT | 2 | Manufacturer | accessdata.fda.gov |
| Pin, Fixation, Smooth | HTY | 2 | Manufacturer, Specification developer | accessdata.fda.gov |
| Staple, Fixation, Bone | JDR | 2 | Manufacturer, 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 |
|---|---|---|---|---|---|---|
| May 29, 2024 | K240049 | LINK(TM) External Fixator | KTT | Substantially Equivalent | Metric Medical Devices, Inc. | accessdata.fda.gov |
| January 13, 2016 | K152627 | IFS Fixation Scaffold System | HTY | Substantially Equivalent | Metric Medical Devices, Inc. | accessdata.fda.gov |
| January 3, 2013 | K123363 | SUPER STAPLE(TM) CLASSIC | JDR | Substantially Equivalent | Metric Medical Devices, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Pin, Fixation, Smooth
- All makers of Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
- All makers of Staple, Fixation, Bone
Updated May 29, 2024. 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.