Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010594946

FEI Number

3010594946

Entity Name

Holocraft Corporation dba Flexcraft Company

City/State/Country

Neptune City, NJ, US

Establishment Address

50 Flexcraft Drive, Neptune City, NJ 07753, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Flexcraft Company (Owner Number: 10044783)

Owner / Operator Contact Address

50 Flexcraft Drive, Neptune City, NJ 07753, 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
KJA	Flask, Tissue Culture	Hematology	Class 1	864.2240	2013-07-29

Official Correspondent

Benjamin Smith

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Flexcraft Company

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 3010594946. Last updated year: 2026. Please use registration number 3010594946 when referencing this establishment in official correspondence.