PressFT

FDA UDI

Class II (US FDA UDI)

by Conmed Corporation

Identity

Trade Name: PressFT FDA UDI
Generic Name: Tendon/ligament bone anchor, non-bioabsorbable FDA UDI
Device Name: PressFT Flex 2.6 PEEK, HIP FDA UDI
Model / Reference: CNP261H FDA UDI
Description: PressFT Flex 2.6 PEEK, HIP FDA UDI

Identifiers

Catalog Number: CNP261H FDA UDI
Primary DI / UDI-DI: 20845854051136 FDA UDI
510(k) Number: K112965 FDA UDI
FDA Product Code: MBI FDA UDI
GMDN Term: Tendon/ligament bone anchor, non-bioabsorbable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3040 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Safe FDA UDI

Category: Tendon/ligament bone anchor, non-bioabsorbable

PressFT by Conmed Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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JuggerKnot Soft Anchors — Biomet Orthopedics, Inc. · Class II
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Cleared under the same submission

K112965 also covers:

PressFT — Conmed Corporation

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Conmed Corporation

Sources (1)

FDA UDI 806992db-ed74-4a9b-ac2d-2fa2637ea68a 38 fields · synced Jun 1, 2026