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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 5 of 7

Device	Model / Reference	Registries	Class	Status
iFix® Interference Screw	CM-1725	FDA UDI	Class II	Active
Quattro®	CM-9002	FDA UDI	Class I	Active
AperFix®	CM-7013	FDA UDI	Class I	Active
Quattro® X Suture Anchor	CM-9255	FDA UDI	Class II	Active
Mirror™	100324	FDA UDI	Class II	Unknown
Quattro®	CM-9509	FDA UDI	Class II	Active
SureLock®	CM-9623	FDA UDI	Class I	Active
BioWick X	CM-6265	FDA UDI	Class II	Active
Mirror™	100315	FDA UDI	Class II	Unknown
AperFix®	CM-7011	FDA UDI	Class I	Active
SureLock®	CM-9640S	FDA UDI	Class I	Active
Mirror™	100300	FDA UDI	Class II	Unknown
AperFix®	CM-7310	FDA UDI	Class I	Active
SureLock®	CM-9620S	FDA UDI	Class I	Active
Mirror™	100298	FDA UDI	Class II	Unknown
AperFix®	CM-7207	FDA UDI	Class I	Active
Quattro®	CM-9202	FDA UDI	Class I	Active
AperFix®	CM-7200	FDA UDI	Class I	Active
SureLock™	CM-9622F	FDA UDI	Class II	Active
BioWick® X	CM-6255	FDA UDI	Class II	Active
Mirror™	100318	FDA UDI	Class II	Unknown
Quattro® X Suture Anchor	CM-9255BGS	FDA UDI	Class II	Active
Drill Guide, Straight, SureLock® 2.2mm	CM9623	FDA UDI	Class I	Active
Quattro®	CM-9007	FDA UDI	Class I	Active
Mirror™	100323	FDA UDI	Class II	Unknown
Quattro®	CM-9005	FDA UDI	Class I	Active
iFix® Interference Screw	CM-1720	FDA UDI	Class II	Active
iFix®	CM-1612	FDA UDI	Class I	Active
AperFix®	CM-7001	FDA UDI	Class I	Active
AperFix®	CM-7109ST	FDA UDI	Class I	Active
Quattro® Link Knotless Anchor	CM-9155	FDA UDI	Class II	Active
AperFix®	CM-7208	FDA UDI	Class I	Active
iFix®	CM-1245	FDA UDI	Class I	Active
iFix®	CM-1830	FDA UDI	Class II	Active
AperFix® Femoral Implant	CM-2909	FDA UDI	Class II	Active
AperFix®	CM-7000	FDA UDI	Class I	Active
Quattro® X Suture Anchor	CM-9265BG	FDA UDI	Class II	Active
Awl/Punch, 4.75/5.5mm Ventix® Link	110025998	FDA UDI	Class I	Active
Accessory Drill Kit, 8mm	CM-9580	FDA UDI	Class I	Active
Tap, Quattro® Suture Anchor 5.5mm	CM9201	FDA UDI	Class I	Active
Drill, 1.4mm SureLock™ All-Suture Anchor	CM9640	FDA UDI	Class I	Active
SureLock®	CM-9641	FDA UDI	Class I	Active
Quattro®	CM-9255BGS	FDA UDI	Class II	Active
Quattro® GL Suture Anchor	CM-9329	FDA UDI	Class II	Active
Quattro®	CM-9500	FDA UDI	Class II	Active
AperFix®	CM-7609	FDA UDI	Class I	Active
Mirror™	100336	FDA UDI	Class II	Unknown
Quattro®	CM-9100	FDA UDI	Class I	Active
AperFix®	CM-7210	FDA UDI	Class I	Active
Mirror™	100322	FDA UDI	Class II	Unknown

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.