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Short SureLock™

FDA UDI

Class II (US FDA UDI)

by Cayenne Medical, Inc.

Identity

Trade Name
Short SureLock™ FDA UDI
Generic Name
Orthopaedic bone screw, non-bioabsorbable, sterile FDA UDI
Device Name
Short SureLock™ All-Suture Anchor, 1.4mm pre-loaded implant (Size 0 Suture) FDA UDI
Model / Reference
CM-961400 FDA UDI
Description
Short SureLock™ All-Suture Anchor, 1.4mm pre-loaded implant (Size 0 Suture) FDA UDI

Identifiers

Primary DI / UDI-DI
M543CM961400 FDA UDI
510(k) Number
K143473 FDA UDI
FDA Product Code
MBI FDA UDI
GMDN Term
Orthopaedic bone screw, non-bioabsorbable, sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Short SureLock™ by Cayenne Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3fc89a87-6a08-4a1d-a710-b583514b351d 35 fields · synced Jun 8, 2026