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Meta-Nail

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
Meta-Nail FDA UDI
Generic Name
Orthopaedic implant aiming arm FDA UDI
Device Name
OFFSET META ANTERIOR DROP FDA UDI
Model / Reference
E0016189-2 FDA UDI
Description
OFFSET META ANTERIOR DROP FDA UDI

Identifiers

Catalog Number
E0016189-2 FDA UDI
Primary DI / UDI-DI
00885556730690 FDA UDI
510(k) Number
K122170 FDA UDI
FDA Product Code
HSB FDA UDI
GMDN Term
Orthopaedic implant aiming arm FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3020 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic implant aiming arm

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

Similar devices

Also classified as Orthopaedic implant aiming arm.

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 4d88a72c-0cb0-4025-86df-4c1f60c8be98 36 fields · synced Jun 8, 2026