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Company · US

Ranfac, Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1985 to 2023. Name variants (Inc, Corp, punctuation) are merged.

16510(k) clearances (0 in 12 months)

0recalls (0 in 12 months)

0recalls that name a 510(k)

Product codes

Code	Device	Records
KNW	Instrument, Biopsy	9
MUU	System, Suction, Lipoplasty	2
FHO	Pneumoperitoneum Needle	1
GAA	Needle, Aspiration And Injection, Disposable	1
GCJ	Laparoscope, General & Plastic Surgery	1
GDF	Guide, Needle, Surgical	1
HET	Laparoscope, Gynecologic (And Accessories)	1

Latest 510(k) clearances

Decided	510(k)	Device and applicant	Code
Feb 21, 2023	K223612	Ranfac Lateral Access Bone Marrow Aspiration Needle (CRVS-BMA-LA) Ranfac Corporation	KNW
Sep 18, 2020	K202287	Ran-Flex-B Bone Marrow Aspiration Needle Ranfac Corporation	KNW
Jun 12, 2019	K190177	J-Type Marrow Biopsy Needle,T-Type Marrow Biopsy Needle,Tweezer Bone Marrow Biopsy Needle, Ranfac Corporation	KNW
Apr 25, 2019	K183146	Ranfac Cartilage Biopsy Needle Ranfac Corporation	KNW
Jan 19, 2017	K162932	Ranfac Fat Aspiration Cannula Ranfac, Corp.	MUU
Oct 19, 2015	K150156	Ranfac Fat Aspiration Transfer Syringe (FATS) Procedure Pack, Ranfac Fat Aspiration Transfer Syringe (FATS) Containment Ranfac, Corp.	MUU
May 22, 2015	K150563	Marrow Cellution Bone Marrow Aspiration Needle Ranfac, Corp.	KNW
Sep 11, 2014	K140991	RANFAC ASPIRATION NEEDLE WITH ADJUSTABLE GUIDE Ranfac, Corp.	KNW
Oct 22, 2013	K131157	RANFAC BONE MARROW ASPIRATION NEEDLE Ranfac, Corp.	KNW
May 23, 2003	K031344	RANFAC GOLDENBERG SNARECOIL SOFT TISSUE BIOPSY (GSS) NEEDLE Ranfac, Corp.	KNW
Aug 22, 2001	K012224	SINGLE ACTION BIOPSY NEEDLE, MODEL RCBS: XX GAUGE, XX LENGTH, XX THROW Ranfac, Corp.	KNW
Aug 9, 1996	K961922	RDP-2 Ranfac, Corp.	HET
Jul 11, 1995	K951090	INTRODUCER Ranfac, Corp.	GCJ
Jul 23, 1993	K930474	NEEDLE, PNEUMOPERITONEUM, SPRING LOADED Ranfac, Corp.	FHO
Nov 5, 1986	K864139	RANFAC CUT BIOPSY NEEDLE Ranfac, Corp.	GAA
Mar 11, 1985	K845038	BREAST & FOREIGN BODY LOCALIZATION INSTRUMENT Ranfac, Corp.	GDF

Latest recalls

Date	Firm and product	Code	Linked 510(k)
No recalls in this window.

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