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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 2 of 7

Device	Model / Reference	Registries	Class	Status
Awl, Quattro® Suture Anchor 5.5/6.5mm	CM9200	FDA UDI	Class I	Active
iFix® Interference Screw	CM-1130	FDA UDI	Class II	Active
iFix®	CM-1720	FDA UDI	Class II	Active
Quattro®	CM-9011	FDA UDI	Class I	Active
Quattro®	CM-9010GT	FDA UDI	Class I	Active
iFix® Interference Screw	CM-1025	FDA UDI	Class II	Active
Quattro®	CM-9329	FDA UDI	Class II	Active
Accessory Drill Kit, 7mm	CM-9570	FDA UDI	Class I	Active
BioWick SureLock®	CM-6101H	FDA UDI	Class I	Active
Quattro®	CM-9255X3	FDA UDI	Class II	Active
AperFix®	CM-7209	FDA UDI	Class I	Active
Quattro®	CM-9010LS	FDA UDI	Class I	Active
AperFix®	CM-2910	FDA UDI	Class II	Active
iFix®	CM-1025	FDA UDI	Class II	Active
SureLock®	CM-9640HS	FDA UDI	Class I	Active
Drill with Centering Sleeve	CM9620S	FDA UDI	Class I	Active
Lock-Stitch® Suture Passer	CM9010LS	FDA UDI	Class I	Active
Quattro®	CM-9148	FDA UDI	Class I	Active
SureLock®	CM-9640H	FDA UDI	Class I	Active
Quattro®	CM-9540	FDA UDI	Class I	Active
Ventix® Link Knotless Anchor	110025990	FDA UDI	Class II	Active
Quattro®	CM-9550	FDA UDI	Class I	Active
Mirror™	100339	FDA UDI	Class II	Unknown
CrossFix®	CM-9300	FDA UDI	Class I	Active
SureLock®	CM-9643	FDA UDI	Class I	Active
AperFix® AM Femoral Implant	CM-2409	FDA UDI	Class II	Active
Quattro®	CM-9004	FDA UDI	Class I	Active
AperFix® Femoral Implant	CM-2911	FDA UDI	Class II	Active
Quattro®	CM-9016	FDA UDI	Class I	Active
Quattro®	CM-9324ST	FDA UDI	Class I	Active
iFix®	CM-1345	FDA UDI	Class I	Active
CrossFix®	CM-8000	FDA UDI	Class I	Active
Tap, for 4.75mm Ventix® Link Knotless Anchor	110026000	FDA UDI	Class I	Active
iFix®	CM-1925	FDA UDI	Class II	Active
Mirror™	100415	FDA UDI	Class II	Unknown
CrossFix® II Disposable Procedure Kit	CM-8000	FDA UDI	Class I	Active
AperFix® AM Femoral Implant	CM-2410	FDA UDI	Class II	Active
Mirror™	100295	FDA UDI	Class II	Unknown
AperFix®	CM-7610	FDA UDI	Class I	Active
Mirror™	100332	FDA UDI	Class II	Unknown
AperFix®	CM-7014	FDA UDI	Class I	Active
iFix®	CM-1030	FDA UDI	Class II	Active
Quattro®	CM-9570	FDA UDI	Class I	Active
iFix®	CM-1130	FDA UDI	Class II	Active
Quattro®	CM-9006	FDA UDI	Class I	Active
Ventix®	110026002	FDA UDI	Class I	Active
Quattro® X3 Triple Loaded Suture Anchor	CM-9255X3	FDA UDI	Class II	Active
AperFix® Femoral Implant	CM-2910	FDA UDI	Class II	Active
iFix®	CM-1920	FDA UDI	Class II	Active
Tap, for 5.5mm Ventix® Link Knotless Anchor	110026001	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.