Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3018071447

FEI Number

3018071447

Entity Name

ADVANCED PRODUCT SOLUTIONS INC.

City/State/Country

Dothan, AL, US

Establishment Address

208 Nypro Lane, Dothan, AL 36305, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

Advanced Product Solutions Inc. (Owner Number: 10080795)

Owner / Operator Contact Address

208 Nypro Lane, Dothan, AL 36305, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Alleset

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FNY	Basin, Emesis	General Hospital	Class 1	880.6730	2021-02-25
FSM	Tray, Surgical, Instrument	General, Plastic Surgery	Class 1	878.4800	2023-03-21
HFW	Clamp, Umbilical	Obstetrics/Gynecology	Class 2	884.4530	2025-08-20
PYB	Minor Surgical Procedures Tray	General, Plastic Surgery	Class 1	878.4800	2024-09-29
HGE	Amniotome	Obstetrics/Gynecology	Class 1	884.4530	2025-08-20
FHG	Bell, Circumcision	Obstetrics/Gynecology	Class 2	884.4530	2025-08-20
KYW	Container, Liquid Medication, Graduated	General Hospital	Class 1	880.6430	2025-01-29
OXQ	Dressing Change Tray	General Hospital	Class 1	880.5075	2025-12-12
OHM	Cesarean Section Tray	Obstetrics/Gynecology	Class 2	884.1720	2025-12-12
FYH	Splint, Extremity, Noninflatable, External, Sterile	General, Plastic Surgery	Class 1	878.3910	2025-07-14
HRH	Trephine, Manual, Ophthalmic	Ophthalmic	Class 1	886.4350	2025-12-12

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Advanced Product Solutions Inc.

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.
Z-0015-2009	Medline Industries Inc	2	Medline Latex Free C-Section CDS-LF and C-Section Supplemental CDS-LF; a single patient prescription procedure pack and disposables, including a Gerber Nuk Pacifier; Made in USA by Medline Industries, Inc., Mundelein, IL 60060
Z-0016-2009	Medline Industries Inc	2	Medline Latex Free Vaginal Delivery CDS-LF; a single patient prescription procedure pack and disposables, including a Gerber Nuk Pacifier; Made in USA by Medline Industries, Inc., Mundelein, IL 60060
Z-0017-2009	Medline Industries Inc	2	Medline Latex Free Labor Kit & Postpartum CDS-LF; a single patient prescription procedure pack and disposables, including a Gerber Nuk Pacifier; Made in USA by Medline Industries, Inc., Mundelein, IL 60060
Z-0018-2009	Medline Industries Inc	2	Medline Latex Free Labor & Delivery CDS-LF; a single patient prescription procedure pack and disposables, including a Gerber Nuk Pacifier; Made in USA by Medline Industries, Inc., Mundelein, IL 60060

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3006487092	ELTEK INSTRUMENTS (PVT.) LTD.	Sialkot Punjab, PK
9613079	WIN WINGS CORP.	SIALKOT Punjab, PK
3004122598	PRODUCTOS MEDLINE S.A. DE C.V.	NUEVO LAREDO Tamaulipas, MX

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3018071447. Last updated year: 2026. Please use registration number 3018071447 when referencing this establishment in official correspondence.