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Data / Medical devices / Laryngoscope, Rigid / United States

FDA-registered makers of Laryngoscope, Rigid in the United States: 45 establishments

45 establishments in the United States are registered with the FDA to make Laryngoscope, Rigid (product code CCW). 4 have a 510(k) clearance or PMA approval on file and 3 have a recall event. FDA data exported November 2, 2026.

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Device
Laryngoscope, Rigid
Product code
CCW
Country
United States

Makers of Laryngoscope, Rigid in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Anesthesia Associates, Inc.San Marcos, CA, United StatesContract manufacturer, Manufacturer, Repackager or relabeler, Specification developer1December 29, 1995000api.fda.gov
Gyrus ACMI, Inc.Brooklyn Park, MN, United StatesComplaint file establishment, Specification developer1October 17, 1988000api.fda.gov
Karl Storz Endoscopy-America, Inc.Auburn, MA, United StatesContract manufacturer, Repackager or relabeler1June 5, 1995000api.fda.gov
Teleflex Medical LLCMorrisville, NC, United StatesComplaint file establishment, Specification developer1November 17, 2006070api.fda.gov
Adroit Surgical LLCOklahoma City, OK, United StatesSpecification developer0000api.fda.gov
Alira Medical Devices LLCRancho Cucamonga, CA, United StatesManufacturer for export0000api.fda.gov
American Diagnostic Corp.Hauppauge, NY, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Bound Tree Medical, LLCGrand Prairie, TX, United StatesManufacturer0000api.fda.gov
CovidienLafayette, CO, United StatesSpecification developer0042api.fda.gov
Dilon Technologies IncNewport News, VA, United StatesManufacturer, Specification developer0000api.fda.gov
Elmed, Inc.Glendale Heights, IL, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Endocraft LLC.Newton, MA, United StatesManufacturer0000api.fda.gov
Fischer Surgical Inc.Imperial, MO, United StatesManufacturer0000api.fda.gov
Geotec, Inc.Warwick, RI, United StatesContract manufacturer0000api.fda.gov
Harwood Design, Inc.Bristol, PA, United StatesContract manufacturer0000api.fda.gov
Icu Medical, Inc.San Clemente, CA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
IntuBlade Co.Lisle, IL, United StatesComplaint file establishment, Manufacturer, Specification developer0000api.fda.gov
Karl Storz Endovision, Inc.Charlton, MA, United StatesContract manufacturer0000api.fda.gov
MEDLINE INDUSTRIES, LP - NorthfieldNorthfield, IL, United StatesSpecification developer0000api.fda.gov
Moldpro Inc.Swanzey, NH, United StatesContract manufacturer0000api.fda.gov
MedSource Labs, LLCChanhassen, MN, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Medline ReNewalRedmond, OR, United StatesReprocessor0000api.fda.gov
National Advanced Endoscopy Devices, Inc.Canoga Park, CA, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
North American Rescue, LLC.Greer, SC, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Nissha Medical Technologies (Ohio), Inc.Norwalk, OH, United StatesContract manufacturer0000api.fda.gov
OBP Medical CorporationLawrence, MA, United StatesSpecification developer0000api.fda.gov
Osi Optoelectronics (medical Division)Hawthorne, CA, United StatesContract manufacturer0000api.fda.gov
One-AI Healthcare, IncRedmond, WA, United StatesComplaint file establishment, Repackager or relabeler, Specification developer0000api.fda.gov
Propper MFG. Co., Inc.Long Island City, NY, United StatesManufacturer, Specification developer0000api.fda.gov
Pure Novamed IncLong Beach, CA, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Primo Medical Group, IncW Bridgewater, MA, United StatesContract manufacturer0000api.fda.gov
Renovo, Inc.Bend, OR, United StatesReprocessor0000api.fda.gov
RG Medical USAMount Juliet, TN, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
Spiracle TechnologyLos Alamitos, CA, United StatesSpecification developer0000api.fda.gov
Salter LabsEl Paso, TX, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
SunMed Group Holdings, LLCGrand Rapids, MI, United StatesComplaint file establishment, Repackager or relabeler, Specification developer0010api.fda.gov
Tidi Products, LLCNeenah, WI, United StatesContract manufacturer0000api.fda.gov
Total Titanium, Inc.Red Bud, IL, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Tri-Anim Health Services, Inc.Dublin, OH, United StatesSpecification developer0000api.fda.gov
Tri-Tech Forensics, Inc.Leland, NC, United StatesSpecification developer0000api.fda.gov
Technimark El PasoEl Paso, TX, United StatesContract manufacturer0000api.fda.gov
Welch Allyn, Inc.Skaneateles Falls, NY, United StatesManufacturer0000api.fda.gov
WM&DGNorthbrook, IL, United StatesSpecification developer0000api.fda.gov
Zien Medical Technologies LLCSalt Lake City, UT, United StatesManufacturer0000api.fda.gov
voss medical productsSan Antonio, TX, United StatesSpecification 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.