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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 1 of 7

Device	Model / Reference	Registries	Class	Status
AperFix®	CM-7270	FDA UDI	Class I	Active
ACL Disposable Procedure Kit	CM-1501	FDA UDI	Class I	Active
Quattro®	CM-9003	FDA UDI	Class I	Active
Quattro® Bolt Tenodesis Screw	CM-9505	FDA UDI	Class II	Active
Quattro®	CM-9129	FDA UDI	Class II	Active
iFix® Interference Screw	CM-1820	FDA UDI	Class II	Active
AperFix®	CM-3009C	FDA UDI	Class II	Active
Quattro® Bolt Tenodesis Screw	CM-9508	FDA UDI	Class II	Active
Quattro®	CM-9145	FDA UDI	Class II	Active
Drill Guide Obturator	CM9302	FDA UDI	Class I	Active
Quattro®	CM-9155	FDA UDI	Class II	Active
AperFix®	CM-7308	FDA UDI	Class I	Active
Mirror™	100343	FDA UDI	Class II	Unknown
Mirror™	100313	FDA UDI	Class II	Unknown
Mirror™	100341	FDA UDI	Class II	Unknown
AperFix®	CM-7611	FDA UDI	Class I	Active
BioWick X®	CM-6201	FDA UDI	Class I	Active
Mirror™	100317	FDA UDI	Class II	Unknown
Quattro®	CM-9203	FDA UDI	Class I	Active
Drill Guide, Curved, SureLock® 2.2mm	CM9625	FDA UDI	Class I	Active
Quattro®	CM-9000UT	FDA UDI	Class I	Active
Quattro®	CM-9000U	FDA UDI	Class I	Active
Mirror™	100342	FDA UDI	Class II	Unknown
Quattro®	CM-8010	FDA UDI	Class I	Active
Quattro®	CM-9012	FDA UDI	Class I	Active
Quattro®	CM-9001	FDA UDI	Class I	Active
iFix® Interference Screw	CM-1925	FDA UDI	Class II	Active
BioWick SureLock®	CM-6120	FDA UDI	Class I	Active
Drill, Hard Bone, for 2.9mm Quattro®	CM-9324ST	FDA UDI	Class I	Active
BioWick X®	CM-6202	FDA UDI	Class I	Active
Quattro®	CM-9145SP	FDA UDI	Class II	Active
Quattro®	CM-9010GTS	FDA UDI	Class I	Active
Drill (Soft Bone), Quattro® Link 4.5mm/5.5mm Anchor	CM9130	FDA UDI	Class I	Active
AperFix®	CM-3008	FDA UDI	Class II	Active
Mirror™	100314	FDA UDI	Class II	Unknown
Accessory Portal Kit, 11mm	CM-7611	FDA UDI	Class I	Active
AperFix®	CM-7010	FDA UDI	Class I	Active
Quattro®	CM-9008	FDA UDI	Class I	Active
Mirror™	100418	FDA UDI	Class II	Unknown
Mirror™	100337	FDA UDI	Class II	Unknown
iFix® Driver, 9-12mm	CM1345	FDA UDI	Class I	Active
Obturator, BioWick™ SureLock®	CM-6121	FDA UDI	Class I	Active
Quattro®	CM-9255BG	FDA UDI	Class II	Active
Quattro®	CM-9580	FDA UDI	Class I	Active
Mirror™	100294	FDA UDI	Class II	Unknown
Quattro®	CM-9508	FDA UDI	Class II	Active
Tibial Implant Removal Tool	CM7300	FDA UDI	Class I	Active
CrossFix® II Meniscal Repair Device	CM8001	FDA UDI	Class II	Active
Ventix®	110025998	FDA UDI	Class I	Active
CrossFix®	CM-8002	FDA UDI	Class II	Active

Related Companies

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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.