FDA Registration Active 🇺🇸 United States

ALTO DEVELOPMENT CORP.

Reg #: 2242056 · FEI: 2242056 · Expires 2026
Products
13
Proprietary Names
14
Establishment Types
3
Classifications
13

Registration Details

Registration Name
ALTO DEVELOPMENT CORP.
Registration Number
2242056
FEI Number
2242056
Status
Active
Expiry Year
2026
Initial Importer
Yes
Address
5206 Asbury Road
City
FARMINGDALE
State
NJ
ZIP
07727
Country
US

Regulatory Submissions

510(k) Number
K181607

Owner / Operator

Firm Name
ALTO DEVELOPMENT CORP.
Operator Number
2242056
Address
5206 Asbury Road
City
Farmingdale
State
NJ
Postal Code
07727
Country
US
Correspondent
Stephanie Schrauder

Products

Device Name Product Code
Plate, Fixation, Bone HRS
Suture, Nonabsorbable, Steel, Monofilament And Multifilament, Sterile GAQ
Screw, Fixation, Bone HWC
Cerclage, Fixation JDQ
Electrode, Pacemaker, Temporary LDF
Tray, Surgical LRP
Punch, Surgical LRY
Suture, Nonabsorbable GAO
Electrosurgical, Cutting & Coagulation & Accessories GEI
Cable, Electrode IKD
Orthopedic Manual Surgical Instrument LXH
Twister, Wire HXS
Instrument, Cutting, Orthopedic HTZ

Proprietary Names

Sternalock® XP Rigid Fixation System MYO/Wire® Ultra-Flex Temporary Pacing Wires BI Series Temporary Pacing Wires Instrument Case Rotating Surgical Punch DoubleWire Sternum Sutures Single Wire Sternum Sutures MYO/Wire® Ultra-Thin Temporary Pacing Wires Electrosurgical Cords Sternal Cable System MYO/Wire® Disposable Patient Cables 2 Crimper/Tensioner Wire Twister Cable Cutter

Establishment Types

Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device Manufacture Medical Device for Another Party (Contract Manufacturer)