SABIN CORPORATION

FDA Device Registration & Listing · Blmgtn, IN, US · Registration 1836564

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
1836564
FEI Number
3003316544
Entity Name
SABIN CORPORATION
City/State/Country
Blmgtn, IN, US
Establishment Address
3800 CONSTITUTION AVE., Blmgtn, IN 47403, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
SABIN CORPORATION (Owner Number: 9045583)
Owner / Operator Contact Address
3800 CONSTITUTION AVE., --, Bloomington, IN 47403, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Needle Percutaneous Entry Needle

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
DWO Needle, Biopsy, Cardiovascular General, Plastic Surgery Class 1 878.4800 2001-04-16
DRC Trocar Cardiovascular Class 2 870.1390 2022-01-10

Official Correspondent

Jayne Frey

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

SABIN CORPORATION
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 1836564. Last updated year: 2026. Please use registration number 1836564 when referencing this establishment in official correspondence.
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