TOBRA MEDICAL, INC.

FDA Device Registration & Listing · Raleigh, NC, US · Registration 3013398027

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3013398027
FEI Number
3013398027
Entity Name
TOBRA MEDICAL, INC.
City/State/Country
Raleigh, NC, US
Establishment Address
3200 Wellington Court, Suite 101, Raleigh, NC 27615, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Complaint File Establishment per 21 CFR 820.198
Owner / Operator
Tobra Medical (Owner Number: 10053159)
Owner / Operator Contact Address
PO Box 1216, Wake Forest, NC 27588, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Tobra FeatherFlow

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
BYY Tube, Aspirating, Flexible, Connecting General Hospital Class 2 880.6740 2023-05-16

Official Correspondent

Bradford Collins

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Tobra Medical
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013398027. Last updated year: 2026. Please use registration number 3013398027 when referencing this establishment in official correspondence.
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