Data / Medical devices / Plug, Punctum / United States
FDA-registered makers of Plug, Punctum in the United States: 11 establishments
11 establishments in the United States are registered with the FDA to make Plug, Punctum (product code LZU). 10 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.
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- Device
- Plug, Punctum
- Product code
- LZU
- Country
- United States
Makers of Plug, Punctum in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Beaver-Visitec International, Inc. | Waltham, MA, United States | Complaint file establishment, Manufacturer, Specification developer | 6 | April 17, 2017 | 0 | 0 | 0 | api.fda.gov |
| Oasis Medical, Inc. | Glendora, CA, United States | Complaint file establishment, Contract manufacturer, Manufacturer | 6 | June 3, 2022 | 0 | 1 | 0 | api.fda.gov |
| Katena Products, Inc. | Parsippany, NJ, United States | Specification developer | 5 | May 2, 2006 | 0 | 0 | 0 | api.fda.gov |
| Katena Products, Inc. | Randolph, NJ, United States | Repackager or relabeler, Specification developer | 4 | July 26, 2002 | 0 | 0 | 0 | api.fda.gov |
| Stephens Instruments, Inc | Lexington, KY, United States | Manufacturer, Repackager or relabeler | 4 | August 28, 2015 | 0 | 0 | 0 | api.fda.gov |
| Medennium, Inc. | Irvine, CA, United States | Manufacturer | 1 | October 18, 2002 | 0 | 0 | 0 | api.fda.gov |
| Microspecialties LLC | Middletown, CT, United States | Manufacturer | 1 | August 19, 2005 | 0 | 0 | 0 | api.fda.gov |
| Nordic Pharma, Inc. | Berwyn, PA, United States | Specification developer | 1 | December 23, 2022 | 0 | 0 | 0 | api.fda.gov |
| Riverpoint Medical LLC | Portland, OR, United States | Manufacturer | 1 | August 28, 2015 | 0 | 0 | 0 | api.fda.gov |
| Summit Medical LLC | Saint Paul, MN, United States | Complaint file establishment, Manufacturer | 1 | May 9, 2003 | 0 | 0 | 0 | api.fda.gov |
| H & W Molding, LLC | Riceboro, GA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. 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.