STINGRAY SURGICAL PRODUCTS

FDA Device Registration & Listing · Boca Raton, FL, US · Registration 3006059917

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3006059917
FEI Number
3006059917
Entity Name
STINGRAY SURGICAL PRODUCTS
City/State/Country
Boca Raton, FL, US
Establishment Address
1701 Costa Del Sol, Boca Raton, FL 33432, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Stingray Surgical Products (Owner Number: 10026274)
Owner / Operator Contact Address
1701 Costa Del Sol, Boca Raton, FL 33432, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Stingray Instrument Trays Stingray Leep/ Lletz Speculum Stingray Instruments Stingray Leep /Lletz Forceps

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FSM Tray, Surgical, Instrument General, Plastic Surgery Class 1 878.4800 2011-02-21
HDF Speculum, Vaginal, Metal Obstetrics/Gynecology Class 1 884.4520 2011-02-21
GEI Electrosurgical, Cutting & Coagulation & Accessories General, Plastic Surgery Class 2 878.4400 2016-11-09
GEG Elevator, Surgical, General & Plastic Surgery General, Plastic Surgery Class 1 878.4800 2011-02-21
HTD Forceps General, Plastic Surgery Class 1 878.4800 2011-02-21

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Stingray Surgical Products
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
K970809 Somnus Medical Technologies, Inc. BENDABLE TISSUE COAGULATING ELECTRODE WITH BENDING TOOL 1997-06-18
K222793 C.R. Bard, Inc. WavelinQ™ Generator 2022-10-17
K002257 Tecno Instruments (Pvt.) , Ltd. TECNO DISPOSABLE FINGERSWITCH PENCIL, MODEL 150-100 2000-10-19
K193591 Bowa-Electronics GmbH & Co. KG ARC 400 2020-04-02
K192128 Sutter Medizintechnik GmbH Sutter Arrowtip Monopolar Electrodes 2019-10-04

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0027-2016 Zimmer, Inc. 1
Zimmer Universal Locking System, Titanium 3.5mm. Zimmer Implant and Instrument Cases are reusable, non-implantable devices designed to facilitate organization, identification, storage, transportation, cleaning, and sterilization processing of reusable instruments and certain unused implantable devices.
Z-0031-06 Rita Medical Systems 2
Rita Brand Habib 4X Electrosurgical Coagulator, Catalog Number: 4401US; Product is distributed by RITA Medical Systems, Inc., One Horizon Way. Manchester, GA 32826

Similar Registrations

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3008886285 Flextronics International Kft Budapest, HU
3012574325 HAKAMA AG Baettwil Solothurn, CH
3001397320 ROECHLING MEDICAL ROCHESTER L.P. Rochester, NY, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3006059917. Last updated year: 2026. Please use registration number 3006059917 when referencing this establishment in official correspondence.
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