Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3040602660

FEI Number

3040602660

Entity Name

REINGENUITY

City/State/Country

Farmingdale, NY, US

Establishment Address

60 Baiting Place Rd, Farmingdale, NY 11735, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Reingenuity (Owner Number: 10084155)

Owner / Operator Contact Address

60 Baiting Place Road, Farmingdale, NY 11735, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K820526

PMA Number

N/A

All Registered Proprietary Names

Honan Balloon

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LCC	Applicator, Ocular Pressure	Ophthalmic	Class 2	886.4610	2022-01-21

Official Correspondent

Robert Reardon Reardon

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Reingenuity

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K852032	Visitec Co.	OCULAR PRESSURE REDUCER (MCCANNEL)	1985-08-12

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1926681	JEDMED Instrument Company	Saint Louis, MO, US
2242450	KATENA PRODUCTS, INC.	Randolph, NJ, US
3028606342	OMAY(GUANGZHOU) MED TECHNOLOGIES CO., LTD	Guangzhou Guangdong, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3040602660. Last updated year: 2026. Please use registration number 3040602660 when referencing this establishment in official correspondence.