FDA Registration Active 🇩🇴 Dominican Republic

OSCOR CARIBE LLC

Reg #: 3004785273 · FEI: 3004785273 · Expires 2026
Products
5
Proprietary Names
21
Establishment Types
2
Classifications
5

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Registration Details

Registration Name
OSCOR CARIBE LLC
Registration Number
3004785273
FEI Number
3004785273
Status
Active
Expiry Year
2026
Initial Importer
No
Address
ZONA FRANCA LAS AMERICAS, NAVE A1-2
City
SANTO DOMINGO Distrito Nacional
Country
DO

Owner / Operator

Firm Name
OSCOR CARIBE LLC
Operator Number
9068575
Address
ZONA FRANCA LAS AMERICAS, NAVE A1-2
City
SANTO DOMINGO
State
Distrito Nacional
Postal Code
11606
Country
DO
Correspondent
Diogenes (DJ) Reyes

US Agent

Business Name
Oscor Inc.
Contact Name
Mohit Malkani
Address
4875 Palm Harbor Blvd
City
Palm Harbor
State
FL
ZIP
34683
Country
US
Phone
727 9372511

Products

Device Name Product Code
Introducer, Catheter DYB
Pacemaker Lead Adaptor DTD
Electrode, Pacemaker, Temporary LDF
Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days FOZ
Probe, Radiofrequency Lesion GXI

Proprietary Names

Destino Twist, Steerable Guiding Catheter BIS/BLV, BLV/BIS Adelante Destino Steerable Guiding Sheath Breezeway II Adelante Sigma, Adelante Sigma AT Adelante Targa INTRO-FLEX SHEATH INTRODUCER W/AMC THROMBOSHIELD TME MULTI-MED CENTRAL VENOUS CATHETERS (CVCS), WITH AND WITHOUT HEPARIN VANTEX CENTRAL VENOUS CATHETERS (CVCS) iLINK BIS Series Adelante Breezeway Delivery Sheath Adelante-S, Adelante-S Lite, Adelante-S2, Adelante-S RS, Adelante SII, SafeSheath II Adelante-S Series Introducer, Adelante Magnum Adelante Destino Adelante Adelante-S, SafeSheath Ultra with VBT Adelante Adelante Radial Disposable RF Electrode Introducer, catheter

Establishment Types

Sterilize Medical Device for Another Party (Contract Sterilizer) Manufacture Medical Device for Another Party (Contract Manufacturer)