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Data / Medical devices / United States / Tender Corporation

Tender Corporation: FDA-registered device maker in Littleton, NH, United States, 8 510(k) clearances

Tender Corporation is registered with the FDA (registration 1250045) in Littleton, NH, United States. It lists 46 device types. The FDA files 8 510(k) clearances under its listings, the newest dated December 1, 2011. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
1250045
Address
944 Industrial Park RD, Littleton, NH, United States, 03561
Owner or operator
Tender Corporation d/b/a Adventure Ready Brands (10034937)
Roles
Complaint file establishment, Manufacturer, Repackager or relabeler, Specification developer
First device listed
January 24, 2011
Registered through
2026
Brand names listed
ACCESSORY, SURGICAL APPAREL, APPLICATOR, ABSORBENT TIPPED, NON-STERILE, After Bite Patch, BANDAGE, CAST, BANDAGE, ELASTIC, BRUSH, SCRUB, OPERATING-ROOM, C-A-T®; C-A-Tourniquet®; Combat Application Tourniquet®, CEMENT, DENTAL and more

Devices it lists

DeviceProduct codeClassRoleSource
Accessory, Surgical ApparelLYU1Repackager or relabeleraccessdata.fda.gov
Airway, NasopharyngealBTQ1Complaint file establishment, Repackager or relabeleraccessdata.fda.gov
Airway, Oropharyngeal, AnesthesiologyCAE1Complaint file establishment, Repackager or relabeler, Specification developeraccessdata.fda.gov
Applicator, Absorbent Tipped, Non-SterileKXF1Repackager or relabeleraccessdata.fda.gov
Bandage, CastITG1Repackager or relabeleraccessdata.fda.gov
Bandage, ElasticFQM1Repackager or relabeleraccessdata.fda.gov
Blade, ScalpelGES1Repackager or relabeleraccessdata.fda.gov
Brush, Scrub, Operating-RoomGEC1Repackager or relabeleraccessdata.fda.gov
Cement, DentalEMA2Repackager or relabeleraccessdata.fda.gov
Continuous Measurement ThermometerFLL2Repackager or relabeleraccessdata.fda.gov
Cotton, RollEFN1Repackager or relabeleraccessdata.fda.gov
Depressor, Tongue, Non-SurgicalFMA1Repackager or relabeleraccessdata.fda.gov
Dressing, Wound, Hydrogel Without Drug And/Or BiologicNAE1Repackager or relabeleraccessdata.fda.gov
Dressing, Wound, HydrophilicNAC1Complaint file establishment, Repackager or relabeler, Specification developeraccessdata.fda.gov
First Aid Kit With DrugLRRNManufacturer, Repackager or relabeleraccessdata.fda.gov
First Aid Kit Without DrugOHO1Manufacturer, Repackager or relabeleraccessdata.fda.gov
Floss, DentalJES1Complaint file establishment, Repackager or relabeleraccessdata.fda.gov
ForcepsHTD1Repackager or relabeleraccessdata.fda.gov
Gauze / Sponge,Nonresorbable For External UseNAB1Repackager or relabeleraccessdata.fda.gov
Hemostatic Wound Dressing Without Thrombin Or Other BiologicsQSYURepackager or relabeleraccessdata.fda.gov
Instrument, Surgical, DisposableKDC1Repackager or relabeleraccessdata.fda.gov
Instruments, Dental HandDZN1Complaint file establishment, Repackager or relabeleraccessdata.fda.gov
Iodine (Tincture)IAL1Complaint file establishment, Repackager or relabeleraccessdata.fda.gov
Latex Patient Examination GloveLYY1Repackager or relabeleraccessdata.fda.gov
Mask, Oxygen, Non-RebreathingKGB1Repackager or relabeleraccessdata.fda.gov
Mirror, MouthEAX1Repackager or relabeleraccessdata.fda.gov
Pack, Hot Or Cold, DisposableIMD1Repackager or relabeleraccessdata.fda.gov
Pad, EyeHMP1Repackager or relabeleraccessdata.fda.gov
Polymer Patient Examination GloveLZA1Repackager or relabeleraccessdata.fda.gov
Protector, Skin PressureFMP1Repackager or relabeleraccessdata.fda.gov
Scissors, Medical, DisposableJOK1Repackager or relabeleraccessdata.fda.gov
Solvent, Adhesive TapeKOX1Repackager or relabeleraccessdata.fda.gov
Splint, Extremity, Non-Inflatable, External, Non-SterileNOC1Repackager or relabeler, Specification developeraccessdata.fda.gov
Splint, Hand, And ComponentsILH1Repackager or relabeler, Specification developeraccessdata.fda.gov
Stapler, SkinQQS1Repackager or relabeleraccessdata.fda.gov
Stethoscope, ManualLDE1Repackager or relabeleraccessdata.fda.gov
Strip, Temperature, Forehead, Liquid CrystalKPD2Repackager or relabeleraccessdata.fda.gov
Syringe, Irrigating (Non Dental)KYZ1Repackager or relabeleraccessdata.fda.gov
Tape And Bandage, AdhesiveKGX1Repackager or relabeleraccessdata.fda.gov
Tape And Bandage, Adhesive, Adjustable Closing Mechanism, Otc UsePYO1Complaint file establishment, Repackager or relabeleraccessdata.fda.gov
Thermometer, Clinical Color ChangeFQZ1Repackager or relabeleraccessdata.fda.gov
Toothbrush, ManualEFW1Repackager or relabeleraccessdata.fda.gov
Tourniquet, NonpneumaticGAX1Repackager or relabeleraccessdata.fda.gov
Valve, Non-RebreathingCBP2Repackager or relabeler, Specification developeraccessdata.fda.gov
Vinyl Patient Examination GloveLYZ1Repackager or relabeleraccessdata.fda.gov
Wax, Dental, IntraoralEGD1Complaint file establishment, Repackager or relabeleraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
December 1, 2011K112126GENUINE FIRST AID CPR MASKCBPSubstantially EquivalentGenuine First Aid, LLCaccessdata.fda.gov
August 24, 2011K110776DIGITAL THERMOMETER MT SERIESFLLSubstantially EquivalentSejoy Electronics & Instruments Co., Ltd.accessdata.fda.gov
April 22, 2010K100855POWDER FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED)LYZSubstantially EquivalentSuzhou Shengyuda Plastic Products Co., Ltd.accessdata.fda.gov
February 26, 2008K072145MEDICAL GLOVE SERIESLYYSubstantially EquivalentZhanjiang Jiali Glove Products Co., Ltd.accessdata.fda.gov
October 16, 2007K072474QUIKCLOT EXQSYSubstantially EquivalentZ-Medica Corporationaccessdata.fda.gov
February 23, 2007K070149POWDER-FREE VINYL PATIENT EXAMINATION GLOVESLYZSubstantially EquivalentWuxi Shenzhou Plastic Products Co., Ltd.accessdata.fda.gov
July 7, 2006K052458LIV MEDICA CPR FACE MASKCBPSubstantially EquivalentLiv Medica Products Pvt. , Ltd.accessdata.fda.gov
May 27, 1993K931084TEMPITEMASubstantially EquivalentCentrix, Inc.accessdata.fda.gov

Compare with other makers

Updated December 1, 2011. 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.