FDA Registration Active 🇺🇸 United States

Domico Med-Device, LLC

Reg #: 3014680784 · FEI: 1825560 · Expires 2026
Products
25
Proprietary Names
9
Establishment Types
4
Classifications
25

Registration Details

Registration Name
Domico Med-Device, LLC
Registration Number
3014680784
FEI Number
1825560
Status
Active
Expiry Year
2026
Initial Importer
Yes
Address
14241 N. Fenton RD
City
Fenton
State
MI
ZIP
48430
Country
US

Owner / Operator

Firm Name
Domico Med-Device
Operator Number
10057806
Address
14241 N. Fenton RD
City
Fenton
State
MI
Postal Code
48430
Country
US
Correspondent
Domico Med-Device

Products

Device Name Product Code
Apparatus, Traction, Non-Powered HST
Mattress, Flotation Therapy, Non-Powered IKY
Table, Radiologic KXJ
Pad, Heating, Powered IRT
Table And Attachments, Operating-Room BWN
Transcranial Magnetic Stimulation System For Obsessive-Compulsive Disorder QCI
Table, Surgical With Orthopedic Accessories, Manual JEB
Lamp, Infrared, Therapeutic Heating ILY
Pediatric Position Holder PRN
Operating Room Accessories Table Tray FWZ
Support, Patient Position CCX
Restraint, Protective FMQ
Accessories, Arthroscopic NBH
Transcranial Magnetic Stimulator OBP
Holder, Head, Radiographic IWY
Stretcher, Hand-Carried FPP
Surgical Table Cushion LWG
Splint, Extremity, Inflatable, External FZF
Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use LXG
Apron, Leaded EAJ
Cassette, Radiographic Film IXA
System, Urine Drainage, Closed, For Nonindwelling Catheter, Sterile EYZ
Table, Operating-Room, Electrical GDC
Device, Transfer, Patient, Manual FMR
Cover, Mattress (Medical Purposes) FMW

Proprietary Names

Cord Management Drape Wedge Cushion Arm Support Cushion Head Cushion Insert Set Med Vac; Arm splints; Child splints; Dual leg splints; Hand, Foot, Wrist, Ankle, Leg Splints; Head splints; Infant Splin Buffing Pad, Arthroscope Arm splints; Child splints; Dual leg splints; Hand, Foot, Wrist, Ankle, Leg Splints; Head splints; Infant Splints Domico Med Vac

Establishment Types

Manufacture Medical Device for Another Party (Contract Manufacturer) Manufacture Medical Device Develop Specifications But Do Not Manufacture At This Facility Complaint File Establishment per 21 CFR 820.198