Data / Medical devices / United States / Advanced Product Solutions Inc.

Advanced Product Solutions Inc.: FDA-registered device maker in Dothan, AL, United States, 1 510(k) clearance

Name: Advanced Product Solutions Inc. FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Advanced Product Solutions Inc. is registered with the FDA (registration 3018071447) in Dothan, AL, United States. It lists 19 device types. The FDA files 1 510(k) clearance under its listings, the newest dated August 24, 2017. Registered through 2027. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Get makers like this one Watch Advanced Product Solutions Inc.

FDA registration number: 3018071447
Address: 208 Nypro Lane, Dothan, AL, United States, 36305
Owner or operator: Advanced Product Solutions Inc. (10080795)
Roles: Contract manufacturer, Repackager or relabeler
First device listed: February 25, 2021
Registered through: 2027
Brand names listed: Alleset, Henry Schein, Invenio, SUN001

Devices it lists

Device	Product code	Class	Role	Source
Accessories, Pump, Infusion	MRZ	2	Repackager or relabeler	accessdata.fda.gov
Amniotome	HGE	1	Contract manufacturer	accessdata.fda.gov
Basin, Emesis	FNY	1	Contract manufacturer	accessdata.fda.gov
Bell, Circumcision	FHG	2	Contract manufacturer	accessdata.fda.gov
Cesarean Section Tray	OHM	2	Contract manufacturer	accessdata.fda.gov
Clamp, Umbilical	HFW	2	Contract manufacturer	accessdata.fda.gov
Container, Liquid Medication, Graduated	KYW	1	Contract manufacturer	accessdata.fda.gov
Dressing Change Tray	OXQ	1	Contract manufacturer	accessdata.fda.gov
General Surgery Tray	LRO	2	Contract manufacturer	accessdata.fda.gov
Instrument, Surgical, Disposable	KDC	1	Contract manufacturer	accessdata.fda.gov
Minor Surgical Procedures Tray	PYB	1	Contract manufacturer	accessdata.fda.gov
Neuraxial Administration Set - Intrathecal Delivery	PYR	2	Repackager or relabeler	accessdata.fda.gov
Oral Surgery Tray	PWL	1	Contract manufacturer	accessdata.fda.gov
Orthopedic Manual Surgical Instrument	LXH	1	Contract manufacturer	accessdata.fda.gov
Pump, Infusion, Pca	MEA	2	Repackager or relabeler	accessdata.fda.gov
Set, Administration, Intravascular	FPA	2	Repackager or relabeler	accessdata.fda.gov
Splint, Extremity, Noninflatable, External, Sterile	FYH	1	Contract manufacturer	accessdata.fda.gov
Tray, Surgical, Instrument	FSM	1	Contract manufacturer	accessdata.fda.gov
Trephine, Manual, Ophthalmic	HRH	1	Repackager or relabeler	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
August 24, 2017	K170982	CADD®- Solis Ambulatory Infusion Pump with Wireless Communication; CADD®-Solis Infusion Pump, Model 2110; PharmGuard® Administrator Medication Safety Software; CADD® Administration Sets; Wireless Communication Module (CM)	MEA	Substantially Equivalent	Smiths Medical Ads, Inc.	accessdata.fda.gov

Compare with other makers

Updated August 24, 2017. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.