MedtechSourcebook

OSCOR INC.

Contract manufacturer and sterilizer · Palm Harbor, FL

FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified

FDA registration
1035166 (openFDA record; or search FDA's registration database)
FEI number
1035166
Registered for
FDA registration year 2026
Establishment types
Complaint file establishment; Manufacturer; Contract manufacturer; Repackager or relabeler; Contract sterilizer
Owner or operator
OSCOR INC. (FDA owner/operator no. 1035166)
Registered address
4875 Palm Harbor Blvd, Palm Harbor, FL 34683
Contract listings
8 device listings, 8 product codes, first listed May 19, 2014
Certification
Not verified. We have no certification data for this facility yet.

Devices listed as contract work

Each row is an FDA product code this facility lists under its contract establishment type, with the date of its earliest such listing.

Product codeDevice (FDA name)ClassCategoryRoleFirst listed
DTBPermanent Pacemaker ElectrodeClass IIICardiovascularContract sterilizationMay 19, 2014
DYBIntroducer, CatheterClass IICardiovascularContract manufacturingMar 7, 2024
GZBStimulator, Spinal-Cord, Implanted (Pain Relief)Class IINeurologyContract manufacturingMar 27, 2015
KYTLight, Examination, Medical, Battery PoweredClass IGeneral hospitalContract sterilizationAug 15, 2017
LGWStimulator, Spinal-Cord, Totally Implanted For Pain ReliefClass IIINeurologyContract manufacturingMay 23, 2022
PSRImplanted Phrenic Nerve Stimulator For Central Sleep ApneaClass IIIAnesthesiologyContract manufacturingOct 18, 2017
PSRImplanted Phrenic Nerve Stimulator For Central Sleep ApneaClass IIIAnesthesiologyContract sterilizationOct 18, 2017
QBIAcute Coronary Syndrome Event DetectorClass IIICardiovascularContract sterilizationJan 10, 2019
QLKStimulator, Neuromuscular, Lower Back Muscles, Totally Implanted For Pain ReliefClass IIINeurologyContract manufacturingJul 1, 2025
QLKStimulator, Neuromuscular, Lower Back Muscles, Totally Implanted For Pain ReliefClass IIINeurologyContract sterilizationJul 1, 2025