Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009702671

FEI Number

3009702671

Entity Name

NEXUS CMF

City/State/Country

Salt Lake City, UT, US

Establishment Address

2825 E. Cottonwood Parkway, Suite 330, Salt Lake City, UT 84121, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility,Complaint File Establishment per 21 CFR 820.198

Owner / Operator

Nexus CMF (Owner Number: 10039882)

Owner / Operator Contact Address

2825 E. Cottonwood Parkway, Suite 330, Salt Lake City, UT 84121, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

TMJ Drape/Fluid Collection Kit Scissors Bone File

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HWT	Template	Orthopedic	Class 1	888.4800	2012-02-17
HTD	Forceps	General, Plastic Surgery	Class 1	878.4800	2017-05-15
NBH	Accessories, Arthroscopic	Orthopedic	Class 1	888.1100	2017-05-15
PUI	Drape, Surgical, Exempt	General, Plastic Surgery	Class 2	878.4370	2022-01-05
HRR	Scissors, Orthopedic, Surgical	Orthopedic	Class 1	888.4540	2021-08-20
HTS	Knife, Orthopedic	Orthopedic	Class 1	888.4540	2017-12-18
GAA	Needle, Aspiration And Injection, Disposable	General, Plastic Surgery	Class 1	878.4800	2017-05-15
HTP	File	Orthopedic	Class 1	888.4540	2021-07-08
HXB	Probe	Orthopedic	Class 1	888.4540	2017-12-13

Official Correspondent

Tiffini Wittwer

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Nexus CMF

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
K852723	The Huxley Instrument Corp.	FOERSTER SPONGE FORCEPS, SERRATED, 7+SS 410 OR 420	1985-07-15
K873512	Arthropedics, Inc.	SERRATED GRASPING FORCEPS, RIGHT	1987-11-02
K781371	Ferris Mfg. Corp.	BONE MARROW ASPIRATION KIT	1978-09-20

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0040-2011	Smith & Nephew, Inc. Endoscopy Division	1	Smith & Nephew Aimer Endofemoral 3mm Offset (Blue) Catalog Number: 72201713 ACUFEX Surgical Instruments are intended for use in orthopedic and general surgery.
Z-0041-2011	Smith & Nephew, Inc. Endoscopy Division	1	Smith & Nephew Aimer Endofemoral 4mm Offset (Purple Catalog Number: 72201714 ACUFEX Surgical Instruments are intended for use in orthopedic and general surgery.
Z-0042-2011	Smith & Nephew, Inc. Endoscopy Division	1	Smith & Nephew Aimer Endofemoral 5mm Offset (Red) Catalog Number: 72201715 ACUFEX Surgical Instruments are intended for use in orthopedic and general surgery.
Z-0043-2011	Smith & Nephew, Inc. Endoscopy Division	1	Smith & Nephew Aimer Endofemoral 6mm Offset (Green) Catalog Number: 72201716 ACUFEX Surgical Instruments are intended for use in orthopedic and general surgery.
Z-0044-2011	Smith & Nephew, Inc. Endoscopy Division	1	Smith & Nephew Aimer Endofemoral 7mm Offset (Gold) Catalog Number: 72201717 ACUFEX Surgical Instruments are intended for use in orthopedic and general surgery.

Similar Registrations

Registration Number	Establishment Name	Location
3030638495	WAREMA KUNSTSTOFFTECHNIK UND MASCHINENBAU GMBH	Marktheidenfeld Bavaria, DE
1835305	Masterbilt Incorporated	South Bend, IN, US
3012130008	MicroPort Orthopedics Global Supply Center Limited	Shanghai, CN
3009631939	RED STAR CONTRACT MANUFACTURING INC.	Larwill, IN, US
9610612	AESCULAP AG	TUTTLINGEN, DONAU Baden-Wurttemberg, DE

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009702671. Last updated year: 2026. Please use registration number 3009702671 when referencing this establishment in official correspondence.