Data / Medical devices / United States / GlobalMed Holdings, LLC
GlobalMed Holdings, LLC: FDA-registered device maker in Scottsdale, AZ, United States, 9 510(k) clearances
GlobalMed Holdings, LLC is registered with the FDA (registration 3004009431) in Scottsdale, AZ, United States. It lists 17 device types. The FDA files 9 510(k) clearances under its listings, the newest dated March 26, 2019. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3004009431
- Address
- 15020 North 74th Street, Scottsdale, AZ, United States, 85260
- Owner or operator
- GlobalMed Holdings, LLC (10033888)
- Roles
- Complaint file establishment, Manufacturer, Repackager or relabeler
- First device listed
- October 14, 2010
- Registered through
- 2026
- Brand names listed
- CAS Lite, Clear Steth, ClearProbe, Interson Simpli Series Ultrasound Probe, ClearProbe; Interson Seemore Ultasound Probe, Clinical Access Station (CAS), ClinicalAccess Pro Connect, First Exam Station, Lite Exam Station and more
Devices it lists
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 |
|---|---|---|---|---|---|---|
| March 26, 2019 | K181658 | MobileECG 2 BT | DSI | Substantially Equivalent | Memtec Corporation | accessdata.fda.gov |
| September 9, 2017 | K170047 | All-in-One Health Monitor, PC-303 | MWI | Substantially Equivalent | Shenzhen Creative Industry Co., Ltd. | accessdata.fda.gov |
| February 21, 2014 | K133509 | EASY PLUS II BLOOD GLUCOSE MONITORING SYSTEM,EASY PLUS II MULTI BLOOD GLUCOSE MONITORING SYSTEM,SMARTEST PERSONA II BLOO | NBW | Substantially Equivalent | Biotest Medical Corp. | accessdata.fda.gov |
| July 10, 2013 | K131338 | DERMA HOOD | PEQ | Substantially Equivalent | Globalmedia Group, LLC | accessdata.fda.gov |
| May 7, 2013 | K130624 | CONI | LLZ | Substantially Equivalent | Globalmed | accessdata.fda.gov |
| February 17, 2012 | K111463 | VALEO VT-601 SERIES IR THERMOMETER | FLL | Substantially Equivalent | Valeo Corp. | accessdata.fda.gov |
| June 6, 2008 | K081032 | TR-USB TELEPHONIC STETHOSCOPE | DQD | Substantially Equivalent | Rnk Products, Inc. | accessdata.fda.gov |
| July 13, 2007 | K063641 | PC-60, NON-INVASIVEPULSE OXIMETER | DQA | Substantially Equivalent | Shenzhen Creative Industry Co., Ltd. | accessdata.fda.gov |
| April 17, 2007 | K070907 | INTERSON USB ULTRASOUND PROBE SYSTEM | IYO | Substantially Equivalent | Regulatory Management Services | accessdata.fda.gov |
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Updated March 26, 2019. 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.