ClearanceBrief
Company ยท US

Sutura, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2000 to 2006. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
GAWSuture, Nonabsorbable, Synthetic, Polypropylene4
OCWEndoscopic Tissue Approximation Device1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Oct 19, 2006K062125SUPERSTITCH 5F, 12F, AND EL
Sutura, Inc.
GAW
Dec 27, 2005K053482SUPERSTITCH GW, MODELS 06-15-04-GW, 08-15-04-GW
Sutura, Inc.
GAW
Apr 17, 2002K020940SUPERSTITCH VASCULAR SUTURING DEVICE, 6 FRENCH, MODELS 06-15-00X; MID-LENGTH 06-25-00X
Sutura, Inc.
GAW
Sep 25, 2001K012865SUPERSTITCH VASCULAR SUTURING DEVICE
Sutura, Inc.
GAW
Mar 1, 2000K994087SUPERSTITCH
Sutura, Inc.
OCW

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
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