Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

9680890

FEI Number

3008501922

Entity Name

RIBBEL INTERNATIONAL LTD.

City/State/Country

SONEPAT Haryana, IN

Establishment Address

20TH MILE JATHERI RD., PO RAI, SONEPAT Haryana 131029, IN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

RIBBEL INTERNATIONAL LTD. (Owner Number: 9039217)

Owner / Operator Contact Address

5a/4a ANSARI ROAD, DARYA GANJ, 3RD FLOOR, NEW DELHI, DELHI, IN-DL 110002, IN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

RIBBEL RIBBEL RIBBEL RIBBEL RIBBEL RIBBEL RIBBEL RIBBEL RIBBEL

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KNX	Collector, Urine, (And Accessories) For Indwelling Catheter	Gastroenterology, Urology	Class 2	876.5250	2017-12-21
GDX	Scalpel, One-Piece	General, Plastic Surgery	Class 1	878.4800	2006-03-20
BYG	Mask, Oxygen	Anesthesiology	Class 1	868.5580	2020-08-15
FZW	Expander, Surgical, Skin Graft	General, Plastic Surgery	Class 1	878.4800	2010-12-29
EME	Punch, Biopsy, Surgical	Dental	Class 1	872.4565	2010-12-29
FZT	Cutter, Surgical	General, Plastic Surgery	Class 1	878.4800	2010-12-29
FZS	Curette, Surgical, General Use	General, Plastic Surgery	Class 1	878.4800	2010-12-29
NNW	Bag, Urine Collection, Leg, For External Use, Non-Sterile	Gastroenterology, Urology	Class 1	876.5250	2018-12-20
GBA	Catheter, Balloon Type	General, Plastic Surgery	Class 1	878.4200	2013-12-25

Official Correspondent

R.K. KANODIA

US Agent Details

DILIP IVOR RAMROOP Business: RAIVANSA INC Email: info@raivansa.com Phone: (718) 7395680

Related Public Records

Same Entity

RIBBEL INTERNATIONAL LTD.

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
K791969	Medline Industries, Inc.	DYNACOR STERILE CLOSED SYS. DRAINAGE BAG	1979-11-05

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0034-2012	X Spine Systems Inc	1	Axle Interspinous Fusion System Torque Driver Handle, Model #: X060-0323, Lot # 525941, S/Ns 001-017, Lot # 525942, S/Ns 001-050, Mfr. By: Bradshaw Medical Inc., Kenosha, WI 53144 The Axle Torque Driver Handle is used to lock the set screw into the locking plate.

Similar Registrations

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1018233	C.R. BARD, INC.	COVINGTON, GA, US
3012445205	AMSINO MEDICAL GROUP (HK) COMPANY LIMITED	HONG KONG, HK
3006082230	C.R. BARD, INC.	MADISON, GA, US
3031582449	JM MEDICAL CO., LTD.	Liaocheng Shandong, CN
3045058049	BOEN HEALTHCARE CO., LTD.	Suzhou Jiangsu, CN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 9680890. Last updated year: 2026. Please use registration number 9680890 when referencing this establishment in official correspondence.