Data / Medical devices / United States / Trident Manufacturing, Inc.

Trident Manufacturing, Inc.: FDA-registered device maker in Pingree Grove, IL, United States, 1 510(k) clearance

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

Trident Manufacturing, Inc. is registered with the FDA (registration 3008717566) in Pingree Grove, IL, United States. It lists 11 device types. The FDA files 1 510(k) clearance under its listings, the newest dated December 8, 2009. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3008717566
Address: 41W275 Railroad Street, Pingree Grove, IL, United States, 60140
Owner or operator: TRIDENT MANUFACTURING, INC. (10029801)
Roles: Contract manufacturer, Manufacturer for export, Repackager or relabeler
First device listed: May 30, 2014
Registered through: 2026
Brand names listed: CM3050: Xact, CM3051: SUTURE DEVICE 5.1, Cypris eXact Suture Placement Device, Cypris eXact Suturing System, Dermapose Access, Dermapose Refresh, Gastrointestinal Anchor Set, ITClamp and more

Devices it lists

Device	Product code	Class	Role	Source
Accessories, Arthroscopic	NBH	1	Contract manufacturer	accessdata.fda.gov
Carrier, Ligature	GEJ	1	Contract manufacturer	accessdata.fda.gov
Clamp, Vascular	DXC	2	Contract manufacturer	accessdata.fda.gov
Device, Fixation, Tracheal Tube	CBH	1	Contract manufacturer	accessdata.fda.gov
Injector, Fluid, Non-Electrically Powered	KZE	2	Manufacturer for export	accessdata.fda.gov
Orthopedic Manual Surgical Instrument	LXH	1	Contract manufacturer	accessdata.fda.gov
Platelet And Plasma Separator For Bone Graft Handling	ORG	2	Contract manufacturer	accessdata.fda.gov
Powered Microneedle Device	QAI	2	Contract manufacturer	accessdata.fda.gov
System, Suction, Lipoplasty	MUU	2	Contract manufacturer	accessdata.fda.gov
System, Suction, Lipoplasty For Removal	QPB	2	Contract manufacturer	accessdata.fda.gov
Tube, Gastro-Enterostomy	KGC	2	Contract manufacturer, 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
December 8, 2009	K093312	KIMBERLY-CLARK GASTROINTESTINAL ANCHOR SET WITH SAF-T-PEXY FASTENERS, ENTERNAL ACCESS DILATION SYSTEM	KGC	Substantially Equivalent	Kimberly-Clark Corp.	accessdata.fda.gov

Compare with other makers

Updated December 8, 2009. 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.