Data / Medical devices / Retractor, Fiberoptic / United States

FDA-registered makers of Retractor, Fiberoptic in the United States: 29 establishments

Name: FDA-registered makers of Retractor, Fiberoptic in the United States
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

29 establishments in the United States are registered with the FDA to make Retractor, Fiberoptic (product code FDG). 1 has 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: Retractor, Fiberoptic
Product code: FDG
Country: United States

Makers of Retractor, Fiberoptic in the United States

Maker	Location	Role	510(k) clearances	Latest clearance	Recall events	Source
Diversatek Healthcare Inc	Milwaukee, WI, United States	Complaint file establishment, Contract manufacturer, Manufacturer, Specification developer	1	February 11, 1997	0	api.fda.gov
Alphatec Spine, Inc.	Carlsbad, CA, United States	Manufacturer	0		0	api.fda.gov
Aspen Surgical Products, Inc.	Caledonia, MI, United States	Complaint file establishment, Specification developer	0		0	api.fda.gov
Alphatec Spine, Inc.	Memphis, TN, United States	Manufacturer	0		0	api.fda.gov
Bioseal	Placentia, CA, United States	Contract manufacturer, Manufacturer, Repackager or relabeler	0		0	api.fda.gov
Black & Black Surgical, Inc.	Tucker, GA, United States	Specification developer	0		0	api.fda.gov
Boss Instruments, Ltd.	Gordonsville, VA, United States	Complaint file establishment, Manufacturer	0		0	api.fda.gov
Centurion Medical Products, LP	Williamston, MI, United States	Specification developer	0		0	api.fda.gov
Flexbar Machine Corp.	Islandia, NY, United States	Specification developer	0		0	api.fda.gov
Gulf Fiberoptics, Inc.	Oldsmar, FL, United States	Manufacturer	0		0	api.fda.gov
Harwood Design, Inc.	Bristol, PA, United States	Contract manufacturer	0		0	api.fda.gov
Highridge Medical, LLC	Westminster, CO, United States	Specification developer	0		0	api.fda.gov
I-Tek Medical, Inc.	White Bear Lake, MN, United States	Contract manufacturer, Manufacturer	0		0	api.fda.gov
Jabil Inc. (Monument)	Monument, CO, United States	Contract manufacturer	0		0	api.fda.gov
KLS-Martin L.P.	Jacksonville, FL, United States	Specification developer	0		0	api.fda.gov
Lumitex Medical Devices, Inc.	Brecksville, OH, United States	Complaint file establishment, Contract manufacturer, Manufacturer	0		1	api.fda.gov
Microport Orthopedics Inc.	Arlington, TN, United States	Repackager or relabeler, Specification developer	0		0	api.fda.gov
Millstone Medical Outsourcing LLC.	Fall River, MA, United States	Contract manufacturer	0		0	api.fda.gov
Millstone Medical Outsourcing LLC	Olive Branch, MS, United States	Contract manufacturer	0		0	api.fda.gov
Olive Branch Distribution Center	Olive Branch, MS, United States	Contract manufacturer	0		0	api.fda.gov
Phoenix Instruments, Inc.	Lisle, IL, United States	Contract manufacturer	0		0	api.fda.gov
Remington Medical, Inc.	Alpharetta, GA, United States	Contract manufacturer	0		0	api.fda.gov
STERIS Corporation	Saint Louis, MO, United States	Manufacturer	0		0	api.fda.gov
Tedan Surgical Innovations, Inc.	Sugar Land, TX, United States	Repackager or relabeler, Specification developer	0		0	api.fda.gov
Teleflex LLC (NADC)	Olive Branch, MS, United States	Manufacturer, Repackager or relabeler	0		0	api.fda.gov
Teleflex Medical LLC	Morrisville, NC, United States	Complaint file establishment, Specification developer	0		0	api.fda.gov
Vitalcor, Inc.	Westmont, IL, United States	Specification developer	0		0	api.fda.gov
West-Conn Tool And Die Inc	Shelton, CT, United States	Contract manufacturer	0		0	api.fda.gov
Weco Manufacturing Group-Henrietta	Rochester, NY, United States	Manufacturer, Repackager or relabeler	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.