Data / Medical devices / United States / 4 Cascade Partners, LLC
4 Cascade Partners, LLC: FDA-registered device maker in Renton, WA, United States, 1 510(k) clearance
4 Cascade Partners, LLC is registered with the FDA (registration 3025231442) in Renton, WA, United States. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated December 22, 2021. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3025231442
- Address
- 618 Smithers Ave S, Renton, WA, United States, 98057
- Owner or operator
- 4 Cascade Partners, LLC (10093094)
- Roles
- Manufacturer
- First device listed
- March 28, 2025
- Registered through
- 2026
- Brand names listed
- Kirkland Signature Brand
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Fentanyl And Other Opioid Protection Glove | QDO | 1 | Manufacturer | accessdata.fda.gov |
| Medical Glove, Specialty | LZC | 1 | Manufacturer | accessdata.fda.gov |
| Polymer Patient Examination Glove | LZA | 1 | Manufacturer | 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 |
|---|---|---|---|---|---|---|
| December 22, 2021 | K211022 | Blue Non Sterile Powder Free Nitrile Examination Gloves, Tested for Use with Chemotherapy Drugs, with Gastric Acid and Fentanyl Permeation Resistance Claims. | LZA | Substantially Equivalent | Central Medicare Sdn Bhd | accessdata.fda.gov |
Compare with other makers
- All makers of Polymer Patient Examination Glove
- All makers of Medical Glove, Specialty
- All makers of Fentanyl And Other Opioid Protection Glove
Updated December 22, 2021. 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.