Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008717566

FEI Number

3008717566

Entity Name

TRIDENT MANUFACTURING, INC.

City/State/Country

Pingree Grove, IL, US

Establishment Address

41W275 RAILROAD STREET, Pingree Grove, IL 60140, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

TRIDENT MANUFACTURING, INC. (Owner Number: 10029801)

Owner / Operator Contact Address

41W275 RAILROAD STREET, Pingree Grove, IL 60140, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

CM3051: SUTURE DEVICE 5.1 Cypris eXact Suturing System Dermapose Access Tropis Gastrointestinal Anchor Set Dermapose Refresh Platelet And Plasma Separator For Bone Graft Handling Cypris eXact Suture Placement Device SkinPen Precision Elite

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GEJ	Carrier, Ligature	General, Plastic Surgery	Class 1	878.4800	2024-02-26
QPB	System, Suction, Lipoplasty For Removal	General, Plastic Surgery	Class 2	878.5040	2020-12-11
KZE	Injector, Fluid, Non-Electrically Powered	General Hospital	Class 2	880.5430	2022-10-18
LXH	Orthopedic Manual Surgical Instrument	Orthopedic	Class 1	888.4540	2026-04-16
KGC	Tube, Gastro-Enterostomy	Gastroenterology, Urology	Class 2	876.5980	2014-05-30
NBH	Accessories, Arthroscopic	Orthopedic	Class 1	888.1100	2026-04-16
MUU	System, Suction, Lipoplasty	General, Plastic Surgery	Class 2	878.5040	2020-12-11
CBH	Device, Fixation, Tracheal Tube	Anesthesiology	Class 1	868.5770	2021-11-22
ORG	Platelet And Plasma Separator For Bone Graft Handling	Hematology	Class 2	864.9245	2024-11-27
GEJ	Carrier, Ligature	General, Plastic Surgery	Class 1	878.4800	2025-09-29
QAI	Powered Microneedle Device	General, Plastic Surgery	Class 2	878.4430	2024-11-26

Official Correspondent

JOHN SAPIENTE

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

TRIDENT MANUFACTURING, 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-0009-2007	Smith & Nephew Inc	1	Journey Nonporous Fin-Stem Tibial Punch, Catalog Numbers: 74018811, 74018813, 74018815, 74018817.
Z-0010-2007	Smith & Nephew Inc	1	Genesis II Nonporous Fin-Stem Tibial Punch, Catalog Numbers: 71440480, 71440482, 71440484, 71440486
Z-0011-06	Stryker Howmedica Osteonics Corp.	1	Allocraft TLIF Bone Inserter.
Z-0011-2007	Smith & Nephew Inc	1	Genesis II Oversized Nonporous Fin-Stem Tibial Punch, Catalog Numbers: 71927102, 71927103, 71927104, 71927105
Z-0013-2011	Depuy Orthopaedics, Inc.	1	Summit Broach Handle, NON-STERILE, MFG: DEPUY ORTHOPAEDICS, INC., PO BOX 988 WARSAW, IN 46581, 1 800 366 8143 Catalog Number: 2570-00-000 The Summit Broach Handle (instrumentation) is used with the DePuy Summit Tapered Hip System. The Broach Handle is used to prepare the femur for hip system implantation. The broach handle is an impaction/extraction device that holds broaches for creating the cavity in the femur during hip arthroplasty.

Similar Registrations

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8040233	QSA SURGICAL (PVT) LTD.	SIALKOT Punjab, PK
3005067367	SHANGHAI MEDICAL INSTRUMENTS (GROUP) LTD. CORP.	Shanghai, CN
1421879	PHOENIX INSTRUMENTS, INC.	Lisle, IL, US
3014644369	International Manufacturing Solutions Operaciones	Cd. Juarez Chihuahua, MX

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008717566. Last updated year: 2026. Please use registration number 3008717566 when referencing this establishment in official correspondence.