Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3016838734

FEI Number

3016838734

Entity Name

NATECH PLASTICS

City/State/Country

Ronkonkoma, NY, US

Establishment Address

85 Remington Blvd., Ronkonkoma, NY 11779, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

NATECH PLASTICS (Owner Number: 10077375)

Owner / Operator Contact Address

85 REMINGTON BLVD., Ronkonkoma, NY 11779, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

ZyMot Multi Sperm Separation Device (850uL)

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MQK	Labware, Assisted Reproduction	Obstetrics/Gynecology	Class 2	884.6160	2020-08-24

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

NATECH PLASTICS

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 3016838734. Last updated year: 2026. Please use registration number 3016838734 when referencing this establishment in official correspondence.