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CAYENNE MEDICAL, INC.

Last updated September 17, 2026

Information

Country: US
Address: 16597 N. 92ND STREET, SCOTTSDALE, AZ, 85260
Website: —
LinkedIn: —
Facebook: —
Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 3006108336
DUNS Number: —

Catalogue (338)

Page 6 of 7

Device	Model / Reference	Registries	Class	Status
Quattro® Bolt Tenodesis Screw	CM-9507	FDA UDI	Class II	Active
Drill (Hard Bone), Quattro® Link 5.5mm Anchor	CM9148	FDA UDI	Class I	Active
Quattro®	CM-9255	FDA UDI	Class II	Active
AperFix®	CM-7255	FDA UDI	Class I	Active
Quattro®	CM-9000QT	FDA UDI	Class I	Active
Lock-Stitch™ Procedure Kit	CM9500	FDA UDI	Class II	Active
Ventix® Link Knotless Anchor	110025992	FDA UDI	Class II	Active
Quattro®	CM-9130	FDA UDI	Class I	Active
Quattro® Q Instrument Tray	CM9000QT	FDA UDI	Class I	Active
Quattro®	CM-9010GT	FDA UDI	Class I	Active
Quattro® Link Knotless Anchor	CM-9145	FDA UDI	Class II	Active
Drill Guide, BioWick™ SureLock®	CM-6120	FDA UDI	Class I	Active
Quattro®	CM-9000Q	FDA UDI	Class I	Active
Quattro®	CM-9015	FDA UDI	Class I	Active
Short SureLock™	CM-961420	FDA UDI	Class II	Unknown
Mirror™	100417	FDA UDI	Class II	Unknown
Mirror™	100299	FDA UDI	Class II	Unknown
SureLock™	CM-9614	FDA UDI	Class II	Active
Tap, Quattro® X3 5.5mm	CM9203	FDA UDI	Class I	Active
Tap, Quattro® Suture Anchor 6.5mm	CM9202	FDA UDI	Class I	Active
Mirror™	100330	FDA UDI	Class II	Unknown
AFX™ Femoral Implant	CM-2509AFX	FDA UDI	Class II	Active
Drill, for 2.9mm Quattro® Link	CM-9300ST	FDA UDI	Class I	Active
Quattro® Bolt Tenodesis Screw	CM-9509	FDA UDI	Class II	Active
SureLock®	CM-9645	FDA UDI	Class I	Active
AperFix®	CM-7110ST	FDA UDI	Class I	Active
AperFix®	CM-1501	FDA UDI	Class I	Active
SureLock®	CM-9625	FDA UDI	Class I	Active
BioWick SureLock	CM-6127	FDA UDI	Class II	Active
Mirror™	100320	FDA UDI	Class II	Unknown
Drill Guide, Curved, SureLock® 1.4mm	CM9645	FDA UDI	Class I	Active
Mirror™	100338	FDA UDI	Class II	Unknown
Quattro®	CM-9265BG	FDA UDI	Class II	Active
Mirror™	100297	FDA UDI	Class II	Unknown
iFix® Interference Screw	CM-1830	FDA UDI	Class II	Active
Hard Bone Drill, for 1.4mm	CM-9640H	FDA UDI	Class I	Active
SureLock® All-Suture Anchor	CM-9622F	FDA UDI	Class II	Active
Ventix™	110025990	FDA UDI	Class II	Active
iFix®	CM-1230	FDA UDI	Class II	Active
Mirror™	100312	FDA UDI	Class II	Unknown
Quattro®	CM-9013	FDA UDI	Class I	Active
Removal Coring Reamer System	CM-7110ST	FDA UDI	Class I	Active
iFix®	CM-1825	FDA UDI	Class II	Active
Quattro®	CM-9301	FDA UDI	Class I	Active
Afx™	CM-2409AP	FDA UDI	Class II	Unknown
AperFix® II Cannulated Tibial System	CM-3011C	FDA UDI	Class II	Active
Drill, for 5.5mm Ventix™ Link Knotless Anchor	110026003	FDA UDI	Class I	Active
Mirror™	100329	FDA UDI	Class II	Unknown
iFix® Interference Screw	CM-1930	FDA UDI	Class II	Active
Drill Guide, Quattro® Suture Anchor 2.9mm	CM9301	FDA UDI	Class I	Active

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FDA Recalls (3)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Date	Recall No.	Class	Status	Reason
Oct 10, 2013	Z-2571-2018	—	terminated	A review of complaints identified a trend for drills breaking.
Jul 11, 2013	Z-2422-2018	—	terminated	Potential for AperFix 24 mm implant breaking inside the drilled femoral socket.
Apr 28, 2010	Z-2548-2018	—	terminated	A review of product complaints in 2010 identified a trend for the Coring Removal Drill of premature wear and/or breakage. This recall occurred in 2013.