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Data / Medical devices / Endoscopic Bite Block / United States

FDA-registered makers of Endoscopic Bite Block in the United States: 26 establishments

26 establishments in the United States are registered with the FDA to make Endoscopic Bite Block (product code MNK). 1 has 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
Endoscopic Bite Block
Product code
MNK
Country
United States

Makers of Endoscopic Bite Block in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Gi SupplyMechanicsburg, PA, United StatesManufacturer1October 4, 1993000api.fda.gov
BiosealPlacentia, CA, United StatesContract manufacturer, Manufacturer, Repackager or relabeler0000api.fda.gov
Boston Scientific CorporationMarlborough, MA, United StatesSpecification developer0000api.fda.gov
Boston Scientific CorporationJohns Creek, GA, United StatesManufacturer0000api.fda.gov
Cordica Medical, Inc.Batavia, IL, United StatesContract manufacturer0000api.fda.gov
Clinical Choice LLCGreensboro, NC, United StatesSpecification developer0000api.fda.gov
Conmed CorporationWestborough, MA, United StatesSpecification developer0000api.fda.gov
Diversatek Healthcare IncMilwaukee, WI, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Dynamic Diagnostics IncorporatedPlymouth, MI, United StatesSpecification developer0000api.fda.gov
Inventeur, LLCSaint Petersburg, FL, United StatesSpecification developer0000api.fda.gov
Kruse Tool & Die, Inc.Warminster, PA, United StatesContract manufacturer0000api.fda.gov
MEDLINE INDUSTRIES, LP - NorthfieldNorthfield, IL, United StatesSpecification developer0000api.fda.gov
Nadia-Health IncDurham, NC, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Nasorcap Medical, Inc.Venetia, PA, United StatesManufacturer0000api.fda.gov
Newtrans International CompanyNashville, TN, United StatesSpecification developer0000api.fda.gov
Nihon Kohden America, Inc.Irvine, CA, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
NeVap Inc Inventory ManagementSan Jose, CA, United StatesSpecification developer0000api.fda.gov
Pneumocyte LLC ( Thoracic Innovations - A Dba Of Pneumocyte)Durham, NC, United StatesSpecification developer0000api.fda.gov
The Lethean Company, LLCChester Sprgs, PA, United StatesManufacturer0000api.fda.gov
Trinity Sterile, Inc.Salisbury, MD, United StatesManufacturer0000api.fda.gov
TeleMed SystemsNorthborough, MA, United StatesSpecification developer0000api.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
United States Endoscopy Group, Inc.Mentor, OH, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Weco Manufacturing Group-HenriettaRochester, NY, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Welmed, Inc.Chicago, IL, 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.