Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

2953195

FEI Number

3001237235

Entity Name

NEOMEND, INC.

City/State/Country

Irvine, CA, US

Establishment Address

60 Technology Dr, Irvine, CA 92618, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Neomend, Inc. (Owner Number: 9030025)

Owner / Operator Contact Address

100 Crossings Blvd, Warwick, RI 02886, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

P150016

All Registered Proprietary Names

Progel Tridyne Tridyne

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NBE	Sealant, Polymerizing	Unknown	Class 3	N/A	2015-02-19
NBE	Sealant, Polymerizing	Unknown	Class 3	N/A	2018-10-19

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Neomend, Inc.

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 2953195. Last updated year: 2026. Please use registration number 2953195 when referencing this establishment in official correspondence.