FDA Registration Active 🇺🇸 United States

TRIDENT MANUFACTURING, INC.

Reg #: 3008717566 · FEI: 3008717566 · Expires 2026
Products
11
Proprietary Names
11
Establishment Types
3
Classifications
11

Registration Details

Registration Name
TRIDENT MANUFACTURING, INC.
Registration Number
3008717566
FEI Number
3008717566
Status
Active
Expiry Year
2026
Initial Importer
No
Address
41W275 RAILROAD STREET
City
Pingree Grove
State
IL
ZIP
60140
Country
US

Regulatory Submissions

510(k) Number
K093312

Owner / Operator

Firm Name
TRIDENT MANUFACTURING, INC.
Operator Number
10029801
Address
41W275 RAILROAD STREET
City
Pingree Grove
State
IL
Postal Code
60140
Country
US
Correspondent
JOHN A SAPIENTE

Products

Device Name Product Code
Carrier, Ligature GEJ
System, Suction, Lipoplasty For Removal QPB
Injector, Fluid, Non-Electrically Powered KZE
Orthopedic Manual Surgical Instrument LXH
Tube, Gastro-Enterostomy KGC
Accessories, Arthroscopic NBH
System, Suction, Lipoplasty MUU
Device, Fixation, Tracheal Tube CBH
Platelet And Plasma Separator For Bone Graft Handling ORG
Powered Microneedle Device QAI
Clamp, Vascular DXC

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 ITClamp CM3050: Xact

Establishment Types

Manufacture Medical Device for Another Party (Contract Manufacturer) Manufacture Device in the United States for Export Only Repack or Relabel Medical Device