Data / Medical devices / Light, Surgical, Ceiling Mounted / United States
FDA-registered makers of Light, Surgical, Ceiling Mounted in the United States: 14 establishments
14 establishments in the United States are registered with the FDA to make Light, Surgical, Ceiling Mounted (product code FSY). 5 have a 510(k) clearance or PMA approval on file and 2 have a recall event. FDA data exported November 3, 2026.
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- Device
- Light, Surgical, Ceiling Mounted
- Product code
- FSY
- Country
- United States
Makers of Light, Surgical, Ceiling Mounted in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Burton Medical LLC | Addison, IL, United States | Complaint file establishment, Manufacturer | 3 | September 30, 2010 | 0 | 0 | 0 | api.fda.gov |
| STRYKER Communications, Inc. | Flower Mound, TX, United States | Complaint file establishment, Manufacturer | 3 | December 30, 2013 | 0 | 14 | 0 | api.fda.gov |
| Medical Illumination International, Inc | Chatsworth, CA, United States | Manufacturer | 1 | August 7, 2014 | 0 | 0 | 0 | api.fda.gov |
| Oricare Inc. | Quakertown, PA, United States | Specification developer | 1 | December 18, 2012 | 0 | 0 | 0 | api.fda.gov |
| Steris Corporation | Montgomery, AL, United States | Complaint file establishment, Manufacturer | 1 | October 5, 2007 | 0 | 0 | 0 | api.fda.gov |
| Aadco Medical, Inc. | Randolph, VT, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Advanced Instrumentations, Inc. | Miami, FL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cardinal Health | Hazelwood, MO, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hill-Rom Company, Inc. | Ladson, SC, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 7 | 0 | api.fda.gov | |
| Klyo Medical Systems Inc | Doral, FL, United States | Manufacturer, Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Linvatec Corporation | Largo, FL, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ondal Medical Systems Of America, Inc. | Sandston, VA, United States | Complaint file establishment, Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Teleflex LLC (NADC) | Olive Branch, MS, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Teleflex Medical LLC | Morrisville, NC, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 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.