Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3006450239

FEI Number

3006450239

Entity Name

CHS USA Incorporated

City/State/Country

PEACHTREE CITY, GA, US

Establishment Address

200 KELLY DRIVE, SUITE A, PEACHTREE CITY, GA 30269, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

CHS USA Incorporated (Owner Number: 9106219)

Owner / Operator Contact Address

200 KELLY DRIVE, SUITE A, --, Peachtree City, GA 30269, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

CHS USA CHS USA CHS USA CHS USA CHS USA CHS USA Minimuffs Nerve Block CHS USA Chest Drain Spinal anesthesia kit Combined Spinal Epidural Anesthesia Kit

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KXF	Applicator, Absorbent Tipped, Non-Sterile	General Hospital	Class 1	880.6025	2024-12-03
FRP	Holder, Infant Position	General Hospital	Class 1	880.5680	2024-12-03
FSM	Tray, Surgical, Instrument	General, Plastic Surgery	Class 1	878.4800	2024-12-03
FMP	Protector, Skin Pressure	General Hospital	Class 1	880.6450	2024-12-03
FON	Bag, Drainage, With Adhesive, Ostomy	Gastroenterology, Urology	Class 1	876.5900	2024-12-03
BYY	Tube, Aspirating, Flexible, Connecting	General Hospital	Class 2	880.6740	2024-12-03
EWE	Protector, Hearing (Circumaural)	Unknown	Class U	N/A	2025-07-17
OGJ	Nerve Block Tray	Anesthesiology	Class 2	868.5140	2025-09-22
FRW	Scale, Patient	General Hospital	Class 1	880.2720	2024-12-03
BSY	Catheters, Suction, Tracheobronchial	Anesthesiology	Class 1	868.6810	2026-03-19
OFU	Spinal Anesthesia Kit	Anesthesiology	Class 2	868.5120	2026-04-30
OFT	Spinal Epidural Anesthesia Kit	Anesthesiology	Class 2	868.5120	2026-04-30

Official Correspondent

Cheryl Brown

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

CHS USA Incorporated

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

View Entity Profile →

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0027-2016	Zimmer, Inc.	1	Zimmer Universal Locking System, Titanium 3.5mm. Zimmer Implant and Instrument Cases are reusable, non-implantable devices designed to facilitate organization, identification, storage, transportation, cleaning, and sterilization processing of reusable instruments and certain unused implantable devices.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006450239. Last updated year: 2026. Please use registration number 3006450239 when referencing this establishment in official correspondence.