Data / Medical devices / United States / Merced Medical, Inc.
Merced Medical, Inc.: FDA-registered device maker in Scottsdale, AZ, United States, 5 510(k) clearances
Merced Medical, Inc. is registered with the FDA (registration 1424478) in Scottsdale, AZ, United States. It lists 77 device types. The FDA files 5 510(k) clearances under its listings, the newest dated May 8, 2018. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 1424478
- FEI number
- 3002902165
- Address
- 9217 E Verde Grove Vw, Scottsdale, AZ, United States, 85255
- Owner or operator
- MERCED MEDICAL, INC. (9039411)
- Roles
- Complaint file establishment
- First device listed
- August 3, 2020
- Registered through
- 2027
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 |
|---|---|---|---|---|---|---|
| May 8, 2018 | K172661 | Fetzer Medical Gynecological Forceps | HCZ | Substantially Equivalent | Fetzer Medical GmbH & Co. KG | accessdata.fda.gov |
| June 29, 2017 | K163524 | Vessel Dilator | DWP | Substantially Equivalent | Fetzer Medical GmbH & Co. KG | accessdata.fda.gov |
| September 9, 2016 | K161004 | Self-retaining Retractor | GZT | Substantially Equivalent | Fetzer Medical GmbH & Co. KG | accessdata.fda.gov |
| February 29, 2016 | K150468 | Laminectomy Rongeurs, Kerrison Rongeurs, IVD Rongeurs | HAE | Substantially Equivalent | K2 Medical GmbH & Co. KG | accessdata.fda.gov |
| April 30, 2012 | K120492 | K2 MEDICAL VASCULAR CLAMPS | DXC | Substantially Equivalent | K2 Medical GmbH & Co. KG | accessdata.fda.gov |
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Updated May 8, 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.