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Data / Medical devices / Light, Surgical, Accessories / United States

FDA-registered makers of Light, Surgical, Accessories in the United States: 21 establishments

21 establishments in the United States are registered with the FDA to make Light, Surgical, Accessories (product code FTA). 5 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
Light, Surgical, Accessories
Product code
FTA
Country
United States

Makers of Light, Surgical, Accessories in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Skytron, LLCGrand Rapids, MI, United StatesComplaint file establishment, Specification developer2April 8, 2014000api.fda.gov
Aspen Surgical Products, Inc.Caledonia, MI, United StatesManufacturer, Repackager or relabeler1February 14, 2002000api.fda.gov
Avid Medical, Inc. A Medical Action Ind. Company 305Toano, VA, United StatesManufacturer, Repackager or relabeler1February 14, 2002000api.fda.gov
Black Diamond Video, Inc.Richmond, CA, United StatesComplaint file establishment, Manufacturer1January 7, 2014000api.fda.gov
Xodus Medical, Inc.New Kensington, PA, United StatesManufacturer1January 19, 2006000api.fda.gov
Alphatec Spine, Inc.Carlsbad, CA, United StatesManufacturer0000api.fda.gov
Alphatec Spine, Inc.Memphis, TN, United StatesManufacturer0000api.fda.gov
Deroyal Industries, Inc.Powell, TN, United StatesComplaint file establishment, Specification developer0000api.fda.gov
DeRoyal Industries, Inc.New Tazewell, TN, United StatesContract manufacturer, Repackager or relabeler0000api.fda.gov
DeRoyal Industries, Inc.Powell, TN, United StatesContract manufacturer0000api.fda.gov
DeRoyal Industries, Inc.Powell, TN, United StatesContract manufacturer, Repackager or relabeler0000api.fda.gov
Litex Manufacturing, Inc.Glendale, CA, United StatesContract manufacturer0000api.fda.gov
MEDLINE INDUSTRIES - MundeleinMundelein, IL, United StatesContract manufacturer0000api.fda.gov
MEDLINE INDUSTRIES, LP - NorthfieldNorthfield, IL, United StatesSpecification developer0000api.fda.gov
Microtek Medical LLCEagan, MN, United StatesSpecification developer0000api.fda.gov
Microtek Medical LLCNorthfield, IL, United StatesSpecification developer0010api.fda.gov
Nelipak PhoenixPhoenix, AZ, United StatesContract manufacturer0000api.fda.gov
Steris CorporationMontgomery, AL, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Toppan Teq LLCHuntley, IL, United StatesContract manufacturer0000api.fda.gov
Teleflex LLC (NADC)Olive Branch, MS, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Teleflex Medical LLCMorrisville, NC, United StatesComplaint file establishment, Specification developer0000api.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.