Registered with FDA

Tender Corporation d/b/a Adventure Ready Brands

Littleton, NH, United States. Lists 7 dental device types with FDA across 1 registered establishment.

FDA owner/operator10034937Repacker / relabeler
Device types listed
7
Brands and models
7
510(k) clearances
0as applicant
Markets registered in
21 registrations outside the US
Establishments
1United States

Registered in 2 markets

Where regulators' registries name Tender Corporation d/b/a Adventure Ready Brands as the manufacturer or the registration holder of a device.

All markets
United States: 7 device types listedCanada: 1 registrations
RegisteredHome: United StatesOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAListerTender Corporation d/b/a Adventure Ready Brands7 device types—Below
CanadaHealth CanadaRegistration holderTENDER CORPORATION12017–2017Pure Global AI

Outside the US the count is of all the company's device registrations in that market, dental or not · matched by company name and country · registry data read 12 Nov 2026

Devices listed with FDA

What Tender Corporation d/b/a Adventure Ready Brands currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Dental Hand InstrumentsDZN · Class 1Dental hand instrumentsLister
Dental Spatula
2022
Mouth MirrorEAX · Class 1Dental hand instrumentsLister
Dental Mirror
2022
Roll CottonEFN · Class 1—Lister
Cotton Roll
2022
Manual ToothbrushEFW · Class 1ToothbrushesLister
TOOTHBRUSH, MANUAL
2017
Intraoral Dental WaxEGD · Class 1—Lister
Dental Wax
2022
Dental CementEMA · Class 2Dental cementsLister
CEMENT, DENTAL
2020
Dental FlossJES · Class 1Floss & interdental cleanersLister
Dental Floss
2022

Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026

Also lists devices cleared under other names

Tender Corporation d/b/a Adventure Ready Brands lists these devices with FDA today. The clearance names a different applicant, as happens after a rename, an acquisition or a private-label agreement.

Original applicants: Centrix, Inc. (1).

Decided510(k)DeviceApplicantDevice type
27 May 1993K931084TEMPITCentrix, Inc.EMA Dental Cement

Registered establishments

EstablishmentLocationWhat it does
Tender CorporationFDA reg. 1250045Littleton, NH, United StatesComplaint file establishment, Repacker / relabeler

Other names on FDA records

Tender Corporation

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10034937). FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record.