Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3003108161

FEI Number

3003108161

Entity Name

QUINTUS, INC.

City/State/Country

Camp Verde, AZ, US

Establishment Address

684 N Industrial Dr, Camp Verde, AZ 86322, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Quintus, Inc. (Owner Number: 10043032)

Owner / Operator Contact Address

684 INDUSTRIAL DRIVE, Camp Verde, AZ 86322, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

VALOR TARGETING GUIDE 4MM CURVED CARBON FIBER RICHARDS EXTERNAL FIXATION SYSTEM 4MM CARBON FIBER ROD 11MM CURVED CARBON FIBE CARBON FIBER RING 11MM CARBON FIBER ROD1 4MM CURVED CARBON FIBER 3MM CARBON FIBER ROD 11MM CUREVED CARBON FIBE 8MM CARBON FIBER ROD SN EXTERNAL FIXATION SYSTEM 8MM CURVED CARBON FIBER BRIDGING ROD JET-X CENTRAL BODY XSHT ASSBY

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HSB	Rod, Fixation, Intramedullary And Accessories	Orthopedic	Class 2	888.3020	2013-01-30
KTT	Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component	Orthopedic	Class 2	888.3030	2013-01-21
KTT	Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component	Orthopedic	Class 2	888.3030	2023-09-11
KTT	Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component	Orthopedic	Class 2	888.3030	2013-03-19
DZL	Screw, Fixation, Intraosseous	Dental	Class 2	872.4880	2013-01-21
KTT	Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component	Orthopedic	Class 2	888.3030	2023-09-11
KTT	Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component	Orthopedic	Class 2	888.3030	2013-01-21
KTT	Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component	Orthopedic	Class 2	888.3030	2013-01-21
LXT	Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, Metal Composite	Orthopedic	Class 2	888.3030	2013-01-21
LXT	Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, Metal Composite	Orthopedic	Class 2	888.3030	2013-01-21
JEY	Plate, Bone	Dental	Class 2	872.4760	2013-01-21
MQN	External Mandibular Fixator And/Or Distractor	Dental	Class 2	872.4760	2023-09-11
LXT	Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, Metal Composite	Orthopedic	Class 2	888.3030	2018-11-19
KTT	Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component	Orthopedic	Class 2	888.3030	2018-11-19
KTT	Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component	Orthopedic	Class 2	888.3030	2013-01-21
LXT	Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, Metal Composite	Orthopedic	Class 2	888.3030	2013-01-21
JDW	Pin, Fixation, Threaded	Orthopedic	Class 2	888.3040	2013-03-19
KTT	Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component	Orthopedic	Class 2	888.3030	2013-01-21
KTT	Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component	Orthopedic	Class 2	888.3030	2017-04-10
JDW	Pin, Fixation, Threaded	Orthopedic	Class 2	888.3040	2013-03-19

Official Correspondent

Stephany Osborn

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Quintus, Inc.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K040336	Synthes (Usa)	SYNTHES (USA) LATERAL ENTRY FEMORAL NAIL SYSTEM	2004-04-12
K083648	Efratgo, Ltd. HI Tech Bio-Surgical	GOTFRIED PHYSIOLOGICAL HIP (PH) NAIL	2009-05-14
K192312	Zimmer GmbH	Zimmer Natural Nail System Cephalomedullary Nails	2019-10-11
K002057	Biomet Orthopedics, Inc.	BROOKER TIBIA NAILS	2000-10-04
K033476	Howmedica Osteonics Corp.	MODIFICATION TO HOFFMANN II MICRO EXTERNAL FIXATION SYSTEM	2004-01-20

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0043-2007	Bioplate Inc	2	Bioplate Resorbable Bone Fixation Tack, Catalog Number: 89-0120, Item Number: SG#-45

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003108161. Last updated year: 2026. Please use registration number 3003108161 when referencing this establishment in official correspondence.