Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3011099779

FEI Number

3011099779

Entity Name

Slater Endoscopy, LLC

City/State/Country

Miramar, FL, US

Establishment Address

10306 USA Today Way, Miramar, FL 33025, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Slater Endoscopy, LLC (Owner Number: 10047312)

Owner / Operator Contact Address

10306 USA Today Way, Miramar, FL 33025, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K150939

PMA Number

N/A

All Registered Proprietary Names

ENSIZOR

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
OCZ	Endoscopic Grasping/Cutting Instrument, Non-Powered	Gastroenterology, Urology	Class 2	876.1500	2016-12-27

Official Correspondent

John Starkey

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Slater Endoscopy, LLC

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
K923489	Cox Medical Ent., Inc.	COX DISPOSABLE RETRIEVAL DEVICES	1992-09-23

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0015-2023	Hobbs Medical, Inc.	2	Hobbs Medical Polypectomy Snare Catalog Number: 4563
Z-0016-2023	Hobbs Medical, Inc.	2	Hobbs Medical Polypectomy Snare Catalog Number: 4564
Z-0026-2023	Hobbs Medical, Inc.	2	Hobbs Helical Retrieval Basket Catalog Number: 4806
Z-0027-2023	Hobbs Medical, Inc.	2	Hobbs Helical Retrieval Basket Catalog Number: 4808
Z-0028-2023	Hobbs Medical, Inc.	2	Hobbs Helical Retrieval Basket Catalog Number: 4814

Similar Registrations

Registration Number	Establishment Name	Location
2011171	Sterigenics US LLC	Los Angeles, CA, US
2936485	STRYKER ENDOSCOPY	SAN JOSE, CA, US
3004837686	Micro-Tech (Nanjing) Co., Ltd.	NAN JING Jiangsu, CN
3006546082	KARL STORZ SE & CO. KG	TUTTLINGEN Baden-Wurttemberg, DE
1000343527	BENTEC Endoscopy GmbH	Rietheim-Weilheim Baden-Wurttemberg, DE

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011099779. Last updated year: 2026. Please use registration number 3011099779 when referencing this establishment in official correspondence.