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Company · US

Anulex Technologies, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2005 to 2012. Name variants (Inc, Corp, punctuation) are merged.

12510(k) clearances (0 in 12 months)

0recalls (0 in 12 months)

0recalls that name a 510(k)

Product codes

Code	Device	Records
GAT	Suture, Nonabsorbable, Synthetic, Polyethylene	4
GZB	Stimulator, Spinal-Cord, Implanted (Pain Relief)	4
MBI	Fastener, Fixation, Nondegradable, Soft Tissue	3
FTL	Mesh, Surgical, Polymeric	1

Latest 510(k) clearances

Decided	510(k)	Device and applicant	Code
Nov 9, 2012	K121356	MICRO/MINI N-PK(H) BONE ANCHOR Anulex Technologies, Inc.	MBI
Nov 9, 2012	K121354	MICRO/MINI N-PK(F) BONE ANCHOR Anulex Technologies, Inc.	MBI
Feb 23, 2012	K113805	FIXATE TISSUE BAND Anulex Technologies, Inc.	GZB
Dec 16, 2011	K113400	FIXATE TISSUE BAND Anulex Technologies, Inc.	GZB
Oct 27, 2011	K112849	FIXATE TISSUE BAND Anulex Technologies, Inc.	GZB
Sep 8, 2011	K111462	FIXATE TISSUE BAND Anulex Technologies, Inc.	GZB
Mar 17, 2010	K100572	VERSACLOSE, MODEL VC-200-01 Anulex Technologies, Inc.	GAT
Jun 12, 2009	K091432	XCLOSE TISSUE REPAIR SYSTEM, MODEL XC-200-01 Anulex Technologies, Inc.	GAT
Dec 19, 2008	K082729	RIMCLOSE BONE ANCHOR Anulex Technologies, Inc.	MBI
Sep 1, 2006	K062307	XCLOSE TISSUE REPAIR SYSTEM, MODEL SRS Anulex Technologies, Inc.	GAT
Jul 5, 2006	K061386	ANCHOR BAND SUTURING SYSTEM, MODEL SR-AB Anulex Technologies, Inc.	GAT
Aug 18, 2005	K050969	INCLOSE SURGICAL MESH SYSTEM Anulex Technologies, Inc.	FTL

Latest recalls

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

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