Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3015542130

FEI Number

3015542130

Entity Name

Nutek Bravo, Hayward

City/State/Country

Hayward, CA, US

Establishment Address

26545 Corporate Ave, Hayward, CA 94545, US

Establishment Type(s)

Sterilize Medical Device for Another Party (Contract Sterilizer)

Owner / Operator

Nutek Bravo (Owner Number: 10081366)

Owner / Operator Contact Address

26545 Corporate Ave, Hayward, CA 94545, 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
KYG	Device, Irrigation, Ocular Surgery	Ophthalmic	Class 1	886.4360	2024-08-01
MGB	Device, Hemostasis, Vascular	Unknown	Class 3	N/A	2023-10-27

Official Correspondent

Thomas Green

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Nutek Bravo

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 3015542130. Last updated year: 2026. Please use registration number 3015542130 when referencing this establishment in official correspondence.