Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3016937081

FEI Number

3016937081

Entity Name

RESCUE SHOT CASE

City/State/Country

Long Branch, NJ, US

Establishment Address

735 Hoey Ave, Long Branch, NJ 07740, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

rescue Shot Case (Owner Number: 10093932)

Owner / Operator Contact Address

735 hoey ave, Long Branch, NJ 07740, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KGB	Mask, Oxygen, Non-Rebreathing	Anesthesiology	Class 1	868.5570	2025-08-09
KPY	Shield, Protective, Personnel	Radiology	Class 1	892.6500	2025-08-09

Official Correspondent

edward shoner

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

rescue Shot Case

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 3016937081. Last updated year: 2026. Please use registration number 3016937081 when referencing this establishment in official correspondence.