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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 3 of 7

Device	Model / Reference	Registries	Class	Status
iFix® Interference Screw	CM-1920	FDA UDI	Class II	Active
AperFix®	CM-2409	FDA UDI	Class II	Active
AperFix®	CM-2909	FDA UDI	Class II	Active
Quattro® Link SP Knotless Anchor	CM-9145SP	FDA UDI	Class II	Active
Quattro®	CM-9138	FDA UDI	Class I	Active
Mirror™	100321	FDA UDI	Class II	Unknown
Mirror™	100335	FDA UDI	Class II	Unknown
iFix®	CM-1820	FDA UDI	Class II	Active
Quattro®	CM-9201	FDA UDI	Class I	Active
AperFix®	CM-7311	FDA UDI	Class I	Active
AperFix®	CM-7300	FDA UDI	Class I	Active
Mirror™	100334	FDA UDI	Class II	Unknown
Short SureLock™	CM-961400	FDA UDI	Class II	Unknown
BioWick® SureLock®	CM-6127	FDA UDI	Class II	Active
Mirror™	100319	FDA UDI	Class II	Unknown
Quattro®	CM-9010GTS	FDA UDI	Class I	Active
Mirror™	100316	FDA UDI	Class II	Unknown
Afx™	CM-2410AP	FDA UDI	Class II	Unknown
Drill with Centering Sleeve	CM9640S	FDA UDI	Class I	Active
Accessory Drill Kit, 6mm	CM-9560	FDA UDI	Class I	Active
Accessory Drill Kit, 5mm	CM-9550	FDA UDI	Class I	Active
SureLock®	CM-9640	FDA UDI	Class I	Active
SureLock®	CM-9620	FDA UDI	Class I	Active
AperFix®	CM-7307	FDA UDI	Class I	Active
Quattro®	CM-9507	FDA UDI	Class II	Active
CrossFix® II Meniscal Repair Device	CM8002	FDA UDI	Class II	Active
Quattro®	CM-9505	FDA UDI	Class II	Active
AperFix®	CM-3010C	FDA UDI	Class II	Active
Femoral Implant Removal Tool	CM7200	FDA UDI	Class I	Active
AperFix®	CM-7250	FDA UDI	Class I	Active
Quattro® X Suture Anchor	CM-9265	FDA UDI	Class II	Active
iFix®	CM-1725	FDA UDI	Class II	Active
AperFix®	CM-7309	FDA UDI	Class I	Active
AperFix®	CM-7211	FDA UDI	Class I	Active
SureLock®	CM-9621	FDA UDI	Class I	Active
Accessory Portal Kit, 10mm	CM-7610	FDA UDI	Class I	Active
Quattro®	CM-9200	FDA UDI	Class I	Active
Tapered Awl/Punch, 4.75/5.5mm Ventix™ Link	110025999	FDA UDI	Class I	Active
AperFix®	CM-7201	FDA UDI	Class I	Active
iFix®	CM-7120	FDA UDI	Class I	Active
Quattro®	CM-9303	FDA UDI	Class I	Active
Quattro® Link Knotless Anchor	CM-9129	FDA UDI	Class II	Active
Quattro®	CM-9560	FDA UDI	Class I	Active
Quattro® X Suture Anchor	CM-9265BGS	FDA UDI	Class II	Active
Mirror™	100327	FDA UDI	Class II	Unknown
Quattro®	CM-9010	FDA UDI	Class I	Active
Quattro® Suture Passer Needle	CM-9011	FDA UDI	Class I	Active
Tap, for 6.5mm BioWick™ X Implant	CM-6202	FDA UDI	Class I	Active
AperFix®	CM-2410	FDA UDI	Class II	Active
iFix® Interference Screw	CM-1030	FDA UDI	Class II	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.