← Back to catalogue

Acumed

FDA UDI

Class II (US FDA UDI)

by Acumed Llc

Identity

Trade Name
ACUMED FDA UDI
Generic Name
Bone nail end-cap FDA UDI
Device Name
FFN +15mm End Cap FDA UDI
Model / Reference
4014-0715 FDA UDI
Description
FFN +15mm End Cap FDA UDI

Identifiers

Primary DI / UDI-DI
10806378116995 FDA UDI
510(k) Number
K143276 FDA UDI
FDA Product Code
HSB FDA UDI
GMDN Term
Bone nail end-cap 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

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Bone nail end-cap

Acumed by Acumed Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone nail end-cap.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Acumed Llc

Sources (1)

  • FDA UDI eecfe944-1035-47b9-b7e6-6a0cbdc2a824 35 fields · synced Jun 1, 2026