Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3016659819

FEI Number

3016659819

Entity Name

PRABADIN CORP

City/State/Country

Miami, FL, US

Establishment Address

13800 SW 119 AVE,, Miami, FL 33186, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198

Owner / Operator

PRABADIN CORP (Owner Number: 10093506)

Owner / Operator Contact Address

13800 SW 119 AVE,, Miami, FL 33186, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Non invasive tubing Anti Embolism Stockings Suction Catheter Disposable Surgical Tray Gauze / sponge,nonresorbable for external use Disposable Surgical Pack

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GAZ	Tubing, Noninvasive	General Hospital	Class 2	880.6740	2026-03-16
DWL	Stocking, Medical Support (To Prevent Pooling Of Blood In Legs)	General Hospital	Class 2	880.5780	2026-03-16
JOL	Catheter And Tip, Suction	General Hospital	Class 2	880.6740	2026-03-16
LRP	Tray, Surgical	General, Plastic Surgery	Class 1	878.4800	2026-03-16
NAB	Gauze / Sponge,Nonresorbable For External Use	General, Plastic Surgery	Class 1	878.4014	2025-05-27
LYU	Accessory, Surgical Apparel	General, Plastic Surgery	Class 1	878.4040	2026-03-16

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

PRABADIN CORP

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
K910471	Baxter Healthcare Corp	MEDID-VAC CLEAR NONCONDUCTIVE CONNECTING TUBE	1991-03-08
K881095	CooperVision, Inc.	KOI(TM) INSTRUMENT TRAYS	1988-04-06

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0007-2013	Invuity, Inc.	2	BriteField illuminated Suction Device; Model numbers 8Fr, 10Fr and 12Fr, Kit (included 8Fr, 10Fr and 12Fr and a sterilization tray. The Invuity Brite Field Illuminated Suction Device is intended to aspirate from the surgical site and to provide illumination from a high intensity light source.
Z-0036-2010	Alphatec Spine, Inc.	1	ROC Lumbar bolt caddy, Part Number: 81997-01-05. Sterilization container for ROC bolts/screws. Product is used to contain spinal implants.

Similar Registrations

Registration Number	Establishment Name	Location
2953726	ADDITION TECHNOLOGY, INC.	Lombard, IL, US
3043534762	AVANTTI MEDI CLEAR MBP, S.A.P.I. DE C.V.	TIJUANA Baja California, MX
3011252788	Changzhou Rongxin Medicine Minimal Invasion Technology Co., Ltd	Jintan Jiangsu, CN
2320762	DEROYAL INDUSTRIES, INC.	NEW TAZEWELL, TN, US
3031231776	Perfect Ophthalmic Instruments FZE	Dubai Dubayy, AE

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3016659819. Last updated year: 2026. Please use registration number 3016659819 when referencing this establishment in official correspondence.