Skip to content

Company · US

Noble Fiber Technologies, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2004 to 2007. Name variants (Inc, Corp, punctuation) are merged.

8510(k) clearances (0 in 12 months)

0recalls (0 in 12 months)

0recalls that name a 510(k)

Product codes

Code	Device	Records
FRO	Dressing, Wound, Drug	4
ISH	Component, External, Limb, Ankle/Foot	1
LGF	Component, Cast	1
MGQ	Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic	1
QSY	Hemostatic Wound Dressing Without Thrombin Or Other Biologics	1

Latest 510(k) clearances

Decided	510(k)	Device and applicant	Code
Aug 21, 2007	K063190	SILVERSEAL WOUND PACKING STRIPS WITH X-STATIC Noble Fiber Technologies, Inc.	QSY
Dec 5, 2005	K050726	SILVERSEAL SILVERAID WITH X-STATIC Noble Fiber Technologies, Inc.	FRO
Jul 21, 2005	K051256	SILVERSEAL ORTHOTIC COMPONENT WITH X-STATIC Noble Fiber Technologies, Inc.	ISH
Jun 13, 2005	K050649	SILVERSEAL CONTACTING WOUND DRESSING WITH X-STATIC Noble Fiber Technologies, Inc.	FRO
Mar 10, 2005	K043526	SILVERSEAL TUBULAR WOUND DRESSING WITH X-STATIC Noble Fiber Technologies, Inc.	LGF
Jan 14, 2005	K033900	X-STATIC SILVERSEAL HYDROCOLLOID FILM AND ISLAND DRESSING Noble Fiber Technologies	FRO
Aug 5, 2004	K033587	SILVERSEAL Noble Fiber Technologies	FRO
Jul 23, 2004	K040019	SILVERSEAL Noble Fiber Technologies	MGQ

Latest recalls

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

Get alerts for these product codes