Data / Medical devices / United States / Rhino Medical Supply Inc

Rhino Medical Supply Inc: FDA-registered device maker in Columbia, SC, United States, 31 510(k) clearances

Name: Rhino Medical Supply Inc FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Rhino Medical Supply Inc is registered with the FDA (registration 3017509841) in Columbia, SC, United States. It lists 17 device types. The FDA files 31 510(k) clearances under its listings, the newest dated August 17, 2023. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3017509841
Address: 649 Rosewood Drive Ste. B, Columbia, SC, United States, 29201
Owner or operator: Rhino Medical Supply Inc (10079910)
Roles: Repackager or relabeler
First device listed: May 24, 2023
Registered through: 2026
Brand names listed: Blunt Fill and Blunt Filter-Ceros, Ceros, Ceros 1 mL Syringe, Ceros Hypodermic Needle, Ceros Needle & Syringe Combo, Ceros Needle Free Vial Access Cannula, Ceros Pre-Filled Flush, Ceros Pro and more

Devices it lists

Device	Product code	Class	Role	Source
Cannula, Injection	FGY	1	Repackager or relabeler	accessdata.fda.gov
Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days	FOZ	2	Repackager or relabeler	accessdata.fda.gov
Container, Liquid Medication, Graduated	KYW	1	Repackager or relabeler	accessdata.fda.gov
Dressing, Wound, Drug	FRO	U	Repackager or relabeler	accessdata.fda.gov
Enteral Syringes With Enteral Specific Connectors	PNR	2	Repackager or relabeler	accessdata.fda.gov
Gastrointestinal Tubes With Enteral Specific Connectors	PIF	2	Repackager or relabeler	accessdata.fda.gov
Gauze/Sponge, Internal	EFQ	U	Repackager or relabeler	accessdata.fda.gov
Needle, Aspiration And Injection, Disposable	GAA	1	Repackager or relabeler	accessdata.fda.gov
Needle, Hypodermic, Single Lumen	FMI	2	Repackager or relabeler	accessdata.fda.gov
Non-Coring (Huber) Needle	PTI	2	Repackager or relabeler	accessdata.fda.gov
Piston Syringe With Neuraxial Connector Epidural, Peripheral, And/Or Indirect Cerebral Spinal Fluid Contact	QEH	2	Repackager or relabeler	accessdata.fda.gov
Polymer Patient Examination Glove	LZA	1	Repackager or relabeler	accessdata.fda.gov
Saline, Vascular Access Flush	NGT	2	Repackager or relabeler	accessdata.fda.gov
Set, Administration, Intravascular	FPA	2	Repackager or relabeler	accessdata.fda.gov
Syringe, Antistick	MEG	2	Repackager or relabeler	accessdata.fda.gov
Syringe, Piston	FMF	2	Repackager or relabeler	accessdata.fda.gov
Tubes, Vials, Systems, Serum Separators, Blood Collection	JKA	2	Repackager or relabeler	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
August 17, 2023	K222773	Feeding Tube	PIF	Substantially Equivalent	Anhui Tiankang Medical Technology Co., Ltd.	accessdata.fda.gov
August 17, 2023	K222772	Oral/Enteral Syringe with ENFit connector	PNR	Substantially Equivalent	Anhui Tiankang Medical Technology Co., Ltd.	accessdata.fda.gov
August 12, 2023	K230756	TK Pre-Filled Normal Saline Flush Syringe	NGT	Substantially Equivalent	Anhui Tiankang Medical Technology Co., Ltd.	accessdata.fda.gov
July 21, 2022	K220184	Pump Alignment Syringe	FMF	Substantially Equivalent	Jiangsu Caina Medical Co.,Ltd	accessdata.fda.gov
July 20, 2022	K214080	Pentaflush	NGT	Substantially Equivalent	Pentaferte Italia S.R.L.	accessdata.fda.gov
July 14, 2022	K220204	Disposabel Syringe with permanently attached needle, Safety Syringe with permanently attached needle	FMF	Substantially Equivalent	Anhui Tiankang Medical Technology Co., Ltd.	accessdata.fda.gov
September 30, 2021	K211593	Enteral Pump Syringe	PNR	Substantially Equivalent	Jiangsu Caina Medical Co.,Ltd	accessdata.fda.gov
May 17, 2021	K210217	Needleless Connector	FPA	Substantially Equivalent	Jiangsu Caina Medical Co.,Ltd	accessdata.fda.gov
May 14, 2021	K210200	1 ml Sterile Hypodermic Syringe For Single Use. With/Without Needle. Luer/Luer-Lock	FMF	Substantially Equivalent	Set Medikal Sanayi VE Ticaret Anonim Sirketi	accessdata.fda.gov
April 7, 2021	K200463	Huber Needle Infusion Set, Safety Huber Needle Infusion Set	PTI	Substantially Equivalent	Jiangsu Caina Medical Co.,Ltd	accessdata.fda.gov
December 14, 2020	K201284	Sterile Hypodermic Syringe for Single Use, with/without needle, luer/luer-lock, Sterile Insulin Syringe for Single Use, with needle, Sterile Hypodermic needle for Single use	FMF	Substantially Equivalent	Set Medikal Sanayi VE Ticaret Anonim Sirketi	accessdata.fda.gov
September 11, 2020	K191639	TK Insulin Syringe with/without Saftey Retractable Device	MEG	Substantially Equivalent	Anhui Tiankang Medical Technology Co., Ltd.	accessdata.fda.gov
September 9, 2020	K200027	Blood Collection Needle with/without Holder, Safety Blood Collection Needle with/without Holder, Luer Access Device-holder with Preattached Multiple Sample Adapter	JKA	Substantially Equivalent	Jiangsu Caina Medical Co.,Ltd	accessdata.fda.gov
August 26, 2020	K200373	Deltaven Fast Flash Closed I.V. Catheter Systems	FOZ	Substantially Equivalent	Delta Med Spa	accessdata.fda.gov
August 11, 2020	K201286	0.9% Sodium Chloride I.V. Flush Syringe for Sterile Delivery, 1 syringe/pouch, 0.9% Sodium Chloride I.V. Flush Syringe for Sterile Delivery, 2 syringes/pouch	NGT	Substantially Equivalent	Nurse Assist, LLC	accessdata.fda.gov
August 6, 2020	K191644	TK Safety Needle	FMI	Substantially Equivalent	Anhui Tiankang Medical Technology Co., Ltd.	accessdata.fda.gov
July 20, 2020	K193022	Retractable Safety Insulin Syringe	MEG	Substantially Equivalent	Jiangsu Caina Medical Co.,Ltd	accessdata.fda.gov
July 17, 2020	K193526	Syringe with safety needle, Safety needle	FMF	Substantially Equivalent	Jiangsu Caina Medical Co.,Ltd	accessdata.fda.gov
January 6, 2020	K191642	TK Sterile Piston Syringe without Needle	FMF	Substantially Equivalent	Anhui Tiankang Medical Technology Co., Ltd.	accessdata.fda.gov
December 19, 2019	K191643	TK Sterile Hypodermic Needle	FMI	Substantially Equivalent	Anhui Tiankang Medical Technology Co., Ltd.	accessdata.fda.gov
October 3, 2019	K191490	Retractable Safety Syringe, Retractable Safety Insulin Syringe, Retractable Safety Tuberculin Syringe, Retractable Safety Allergy Syringe	MEG	Substantially Equivalent	Jiangsu Caina Medical Co.,Ltd	accessdata.fda.gov
August 6, 2019	K190502	ENFit Oral / Enteral Syringe	PNR	Substantially Equivalent	Jiangsu Caina Medical Co.,Ltd	accessdata.fda.gov
December 14, 2018	K181374	NRFit Syringe	QEH	Substantially Equivalent	Jiangsu Caina Medical Co.,Ltd	accessdata.fda.gov
June 14, 2018	K172938	Disposable Sterile Needle	FMI	Substantially Equivalent	Jiangsu Caina Medical Co.,Ltd	accessdata.fda.gov
March 22, 2017	K161979	ENFit enteral syringe	PNR	Substantially Equivalent	Jiangyin Caina Technology Co., Ltd.	accessdata.fda.gov
August 31, 2015	K150143	Normal Saline Flush	NGT	Substantially Equivalent	Nurse Assist, Inc.	accessdata.fda.gov
May 12, 2014	K131531	TIANKANG DISPOSABLE SYRINGES WITH RE-USE PREVENTION FEATURE WITH OR WITHOUT NEEDLE	MEG	Substantially Equivalent	Anhui Tiankang Medical Products Co., Ltd.	accessdata.fda.gov
August 3, 2012	K121526	POWER-FREE NITRILE PATIENT EXAMINATION GLOVES	LZA	Substantially Equivalent	Shandong Junchi Medical Products Co., Ltd.	accessdata.fda.gov
December 18, 2008	K083042	WOUND FLUSH, STERILE WATER & NORMAL SALINE	FRO	Substantially Equivalent	Nurse Assist, Inc.	accessdata.fda.gov
January 11, 2001	K002381	PENTAFERTE SINGLE USE SYRINGES, MODEL SIZE=VARIOUS SIZES	FMF	Substantially Equivalent	Pentaferte, S.R.L.	accessdata.fda.gov
November 5, 1979	K791871	NEUROLOGICAL SPONGES (PATTIES)	EFQ	Substantially Equivalent	Carwild Corp.	accessdata.fda.gov

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Updated August 17, 2023. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.