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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: —
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Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 3006108336
DUNS Number: —

Catalogue (338)

Page 7 of 7

Device	Model / Reference	Registries	Class	Status
Mirror™	100301	FDA UDI	Class II	Unknown
iFix® Interference Screw	CM-1230	FDA UDI	Class II	Active
Removal Coring Reamer System	CM-7109ST	FDA UDI	Class I	Active
Accessory Drill Kit, 4mm	CM-9540	FDA UDI	Class I	Active
BioWick SureLock®	CM-6121	FDA UDI	Class I	Active
Mirror™	100331	FDA UDI	Class II	Unknown
AFX™ Femoral Implant	CM-2510AFX	FDA UDI	Class II	Active
Mirror™	100296	FDA UDI	Class II	Unknown
Mirror™	100333	FDA UDI	Class II	Unknown
iFix® Interference Screw	CM-1825	FDA UDI	Class II	Active
Drill Tip Guide Wire (14")	CM-7014	FDA UDI	Class I	Active
AperFix® II Cannulated Tibial System	CM-3009C	FDA UDI	Class II	Active
Mirror™	100326	FDA UDI	Class II	Unknown
Obturator, SureLock® 1.4mm	CM9641	FDA UDI	Class I	Active
iFix®	CM-1930	FDA UDI	Class II	Active
Aperfix Interference Screw 7-12 Mm X 20 Mm; 7-12 Mm X 25 Mm; 7-12 Mm X 30 Mm	K073426	FDA 510(k)	Class II	Active
Crossfix Ii Memiscal Repair Device	K121413	FDA 510(k)	Class II	Active
AFX Femoral Implant with Inserter	K192428	FDA 510(k)	Class II	Active
Short SureLock All-Suture Anchor, 1.4mm with (1) size 0 UHMWPE suture with needles, Short SureLock All-Suture Anchor, 1.4mm with (1) size 2-0 UHMWPE suture with needles	K143473	FDA 510(k)	Class II	Active
BioWick X Implant with Driver	K172186	FDA 510(k)	Class II	Active
Modification To Aperfix Femoral Implant With Inserter	K073054	FDA 510(k)	Class II	Active
Quattro Gl Suture Anchor	K131325	FDA 510(k)	Class II	Active
Ventix Link Knotless Anchor with Inserter	K180274	FDA 510(k)	Class II	Active
SureLock W Suture Anchor	K151068	FDA 510(k)	Class II	Active
Dual Needle Suture Passer System	K082518	FDA 510(k)	Class II	Active
Aperfix Am Femoral Implant With Inserter, 9x24 Aperfix Am Femoral Implant With Inserter, 10x24 Aperfix Femoral Implant W	K122463	FDA 510(k)	Class II	Active
Labralink Suture Anchor With Inserter, 2.9mm Per-Loaded With One (1) And (2) #2 Uhmwpe Suture	K112960	FDA 510(k)	Class II	Active
Quattro Bolt Tenodesis Screw	K143392	FDA 510(k)	Class II	Active
Aperfix Implant With Inserter, 8, 9, 10, 11, Mm X30 Mm	K083607	FDA 510(k)	Class II	Active
Capsew Plication System	K071796	FDA 510(k)	Class II	Active
Aperfix Tibial Implant With Inserter	K063070	FDA 510(k)	Class II	Active
Aperfix Femoral Implant With Inserter	K062487	FDA 510(k)	Class II	Active
Cufflink(tm) Knotless Anchor With Inserter, 4.5mm/5.5mm - Peek Only, Cufflink Sp(tm) Knotless Anchor With Inserter, 4.5	K112876	FDA 510(k)	Class II	Active
AFX™ Femoral Implant With Inserter	K161033	FDA 510(k)	Class II	Active
Aperfix Femoral Implant With Inserter, 9, 10, 11 Mm X 35mm And X 29mm	K083612	FDA 510(k)	Class II	Active
Quatro Link Knotless Anchor With Inserter, 2.9mm-Peek Only	K122314	FDA 510(k)	Class II	Active
Cuffink	K112814	FDA 510(k)	Class II	Active
Surelock All-Suture Anchor With Inserter, 1.4mm, Surelock All-Suture Anchor With Inserter, 2.2mm	K132867	FDA 510(k)	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.