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Sign in to claim this brandMESA LABORATORIES, INC.
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 12100 W 6th Ave, Denver, CO, 80228
- Website
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- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 1720309
- DUNS Number
- —
Catalogue (108)
Page 3 of 3| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Conductivity/Tds Calibrator Solution | K033330 | FDA 510(k) | Class II | Active |
| Sterrad Cyclesure 24 Plus Biological Indicator | K140589 | FDA 510(k) | Class II | Active |
| Phoenix XL Dialysate Meter | K150657 | FDA 510(k) | Class II | Active |
| SmartHDM-510 System | K201765 | FDA 510(k) | Class II | Active |
| Comined Standard Solution | K130100 | FDA 510(k) | Class II | Active |
| Smart-Well Incubator | K122362 | FDA 510(k) | Class II | Active |
| TDS Standard Solution | K191496 | FDA 510(k) | Class II | Active |
| 90xl Instrumentation System | K050812 | FDA 510(k) | Class II | Active |
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FDA Recalls (3)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| May 12, 2017 | Z-2159-2017 | — | terminated | Mesa Laboratories is recalling Conductivity/TDS Calibrator Solution due to failure to meet product specifications. |
| Apr 4, 2016 | Z-1104-2017 | — | terminated | Product resistance has fallen outside of label claim within expiry. |
| Sep 13, 2013 | Z-0175-2014 | — | terminated | Mesa Laboratories, Inc. is recalling certain lots of pH 7.0 Buffer Solution due to mold growth. |