Data / Medical devices / United States / StringKing
StringKing: FDA-registered device maker in Carson, CA, United States, 1 510(k) clearance
StringKing is registered with the FDA (registration 3021450335) in Carson, CA, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated April 23, 2021. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3021450335
- Address
- 1005 E Artesia Blvd, Carson, CA, United States, 90746
- Owner or operator
- String King Lacrosse, LLC (10075863)
- Roles
- Manufacturer
- First device listed
- June 29, 2020
- Registered through
- 2026
- Brand names listed
- DIG.SMS.L2.BLU, Disposable Isolation Gown - Level 2, Disposable Isolation Gown - Level 2 - SMS, Polyethylene Isolation Gown Level 2, Procedure Mask - Level 3, Protective Gown - PE, Protective Gown - PE - Thumb Loop, Protective Gown - PP/PE and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Mask, Surgical | FXX | 2 | Manufacturer | accessdata.fda.gov |
| Non-Surgical Gown | OEA | 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 |
|---|---|---|---|---|---|---|
| April 23, 2021 | K202607 | Surgical Mask - Level 3 - Blue - 50 pcs, Surgical Mask - Level 3 - White - 50 pcs, Procedure Mask - Level 3 - Blue - 50 pcs, Procedure Mask - Level 3 - White - 50 pcs | FXX | Substantially Equivalent | String King Lacrosse, LLC | accessdata.fda.gov |
Compare with other makers
Updated April 23, 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.