Slessinger Enterprises

FDA Device Registration & Listing · New York, NY, US · Registration 3011461072

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
3011461072
FEI Number
3011461072
Entity Name
Slessinger Enterprises
City/State/Country
New York, NY, US
Establishment Address
530 E 72nd St Apt 2f, New York, NY 10021, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Slessinger Enterprises LLC (Owner Number: 10048682)
Owner / Operator Contact Address
530 East 72nd St, Apt 2F, New York, NY 10021, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

CT/MR Slessinger Board for HDR Brachytherapy

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IKX Aid, Transfer Physical Medicine Class 1 890.5050 2015-02-11

Official Correspondent

Eric Slessinger

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Slessinger Enterprises LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011461072. Last updated year: 2026. Please use registration number 3011461072 when referencing this establishment in official correspondence.
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