Data / Medical devices / Lamp, Surgical / United States
FDA-registered makers of Lamp, Surgical in the United States: 14 establishments
14 establishments in the United States are registered with the FDA to make Lamp, Surgical (product code FTD). 3 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Lamp, Surgical
- Product code
- FTD
- Country
- United States
Makers of Lamp, Surgical in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| BihlerMed, LLC | Phillipsburg, NJ, United States | Manufacturer | 2 | December 5, 2013 | 0 | 0 | 0 | api.fda.gov |
| Atricure, Inc. | Mason, OH, United States | Manufacturer | 1 | June 9, 2011 | 0 | 0 | 0 | api.fda.gov |
| Stryker Puerto Rico, LLC. | Arroyo, PR, United States | Manufacturer | 1 | June 30, 1998 | 0 | 0 | 0 | api.fda.gov |
| Biotex, Inc. | Houston, TX, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Groman Inc. | Coconut Creek, FL, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hosmed Inc. | Doral, FL, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hill-Rom Company, Inc. | Ladson, SC, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Klyo Medical Systems Inc | Doral, FL, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Mezlight, LLC | Madison, WI, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Qed, Inc. | Lexington, KY, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Red Star Contract Manufacturing Inc. | Larwill, IN, United States | 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 | |
| Tiger Aesthetics Medical-SD | San Diego, CA, United States | Complaint file establishment, Manufacturer, Specification developer | 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.