Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008785630

FEI Number

3008785630

Entity Name

KERYLOS CORPORATION

City/State/Country

Reno, NV, US

Establishment Address

4225 Longknife Road, Reno, NV 89519, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

KERYLOS CORPORATION (Owner Number: 10034078)

Owner / Operator Contact Address

4225 Longknife Road, Reno, NV 89519, 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
FGY	Cannula, Injection	General, Plastic Surgery	Class 1	878.4200	2010-11-03
GEA	Cannula, Surgical, General & Plastic Surgery	General, Plastic Surgery	Class 1	878.4800	2010-11-03

Official Correspondent

Cyril Sebban

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

KERYLOS CORPORATION

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
K863293	Lifestream Int'L, Inc.	DISPOSABLE SUCTION CANNULA NO. 902008-000	1986-09-09

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0019-2023	Hobbs Medical, Inc.	1	Hobbs Scope Introducer Catalog Number: 4650

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008785630. Last updated year: 2026. Please use registration number 3008785630 when referencing this establishment in official correspondence.