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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 4 of 7

Device	Model / Reference	Registries	Class	Status
AperFix®	CM-7111ST	FDA UDI	Class I	Active
Mirror™	100340	FDA UDI	Class II	Unknown
AperFix®	CM-3011C	FDA UDI	Class II	Active
Awl, Quattro® Knotless Anchor 4.5/5.5mm	CM9100	FDA UDI	Class I	Active
Accessory Portal Kit, 9mm	CM-7609	FDA UDI	Class I	Active
AperFix®	CM-2911	FDA UDI	Class II	Active
Mirror™	100416	FDA UDI	Class II	Unknown
Drill, for 4.75mm Ventix™ Link Knotless Anchor	110026002	FDA UDI	Class I	Active
Ventix™	110025992	FDA UDI	Class II	Active
Quattro®	CM-9506	FDA UDI	Class II	Active
Obturator, SureLock® 2.2mm	CM9621	FDA UDI	Class I	Active
AperFix® II Cannulated Tibial System	CM-3010C	FDA UDI	Class II	Active
Quattro®	CM-9329GL2	FDA UDI	Class II	Active
Quattro® Bolt Tenodesis Screw	CM-9506	FDA UDI	Class II	Active
Ventix®	110026000	FDA UDI	Class I	Active
SureLock® All-Suture Anchor	CM-9614F	FDA UDI	Class II	Active
Ventix®	110026001	FDA UDI	Class I	Active
SureLock™	CM-9622	FDA UDI	Class II	Active
Quattro®	CM-9014	FDA UDI	Class I	Active
Guide Wire Ø 2.4mm, 2- Flute	CM7013	FDA UDI	Class I	Active
CrossFix®	CM-8001	FDA UDI	Class II	Active
Drill, 2.2mm SureLock™ All-Suture Anchor	CM9620	FDA UDI	Class I	Active
Quattro®	CM-9009	FDA UDI	Class I	Active
Hard Bone Drill, with Centering Sleeve	CM9640HS	FDA UDI	Class I	Active
Quattro®	CM-9265	FDA UDI	Class II	Active
BioWick X	CM-6255	FDA UDI	Class II	Active
Mirror™	100325	FDA UDI	Class II	Unknown
Quattro® X Suture Anchor	CM-9255BG	FDA UDI	Class II	Active
Tap, for 5.5mm BioWick™ X Implant	CM-6201	FDA UDI	Class I	Active
Drill, 2.7mm, for BioWick™ SureLock™	CM6101	FDA UDI	Class I	Active
SureLock™	CM-9614F	FDA UDI	Class II	Active
Mirror™	100414	FDA UDI	Class II	Unknown
Quattro®	CM-9300ST	FDA UDI	Class I	Active
BioWick SureLock®	CM-6101	FDA UDI	Class I	Active
Offset Drill Guide, Quattro® Link 2.9mm	CM9303	FDA UDI	Class I	Active
Ventix®	110026003	FDA UDI	Class I	Active
iFix® Driver, 7-8mm	CM1245	FDA UDI	Class I	Active
Removal Coring Reamer System	CM-7111ST	FDA UDI	Class I	Active
Hard Bone Drill, for 2.7mm	CM-6101H	FDA UDI	Class I	Active
AperFix®	CM-7260	FDA UDI	Class I	Active
BioWick® X	CM-6265	FDA UDI	Class II	Active
Quattro®	CM-9265BGS	FDA UDI	Class II	Active
AperFix® II Tibial System	CM-3008	FDA UDI	Class II	Active
Drill (Hard Bone), Quattro® Link 4.5mm / SP Anchor	CM9138	FDA UDI	Class I	Active
Quattro® Suture Passer	CM-9010	FDA UDI	Class I	Active
Drill Guide, Straight, SureLock® 1.4mm	CM9643	FDA UDI	Class I	Active
Quattro®	CM-9302	FDA UDI	Class I	Active
Mirror™	100328	FDA UDI	Class II	Unknown
Quattro® GL2 Suture Anchor	CM-9329GL2	FDA UDI	Class II	Active
Ventix®	110025999	FDA UDI	Class I	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.