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Twinfix

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
TWINFIX FDA UDI
Generic Name
Tendon/ligament bone anchor, non-bioabsorbable FDA UDI
Device Name
TWINFIX 2.8 MM TITANIUM SUTURE ANCHOR WITH ONE No.2 PRELOADED DURABRAID SUTURE STERILE FDA UDI
Model / Reference
72200762 FDA UDI
Description
TWINFIX 2.8 MM TITANIUM SUTURE ANCHOR WITH ONE No.2 PRELOADED DURABRAID SUTURE STERILE FDA UDI

Identifiers

Catalog Number
72200762 FDA UDI
Primary DI / UDI-DI
03596010584458 FDA UDI
510(k) Number
K152566 FDA UDI
K972326 FDA UDI
FDA Product Code
JDR FDA UDI
MBI FDA UDI
GMDN Term
Tendon/ligament bone anchor, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 FDA UDI
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

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

No

FDA UDI

Category: Tendon/ligament bone anchor, non-bioabsorbable

Twinfix by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tendon/ligament bone anchor, non-bioabsorbable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fd6ee2ee-46c4-4bd9-ba84-f7b6c8f7a90e 36 fields · synced Jun 8, 2026