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Acumed 3014-23036

by Acumed LLC

Ref 3014-23036

Acumed 3014-23036 is a device classified as Class IIa in the EU and Class II in the US made by Acumed LLC, registered in EUDAMED on 29 Oct 2026 (Basic UDI-DI B-10806378096778), cleared under FDA 510(k) K143394 on 23 Jan 2015 and listed in FDA GUDID since 24 Oct 2015 (UDI-DI 10806378096778), active as of 7 Nov 2026.

Active European Union and United States. Also listed in GUDID (US).

CE MDD 510(k)

Valid until

No date given

CE: no date in EUDAMED. FDA: not time-limited

FDA recalls

None found

in data synced 7 Nov 2026

Documents

None linked in EUDAMED

A group certificate may exist

510(k) K143394

FDA submission, from GUDID

Trust

Unverified

Source EUDAMED, GUDID, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-10806378096778 Basic UDI-DI 10806378096778UDI-DIDate29 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10806378096778 UDI-DI Date24 Oct 2015ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE GUDID from GUDID Substantially Equivalent · Traditional NumberK143394 Date23 Jan 2015DecidedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI B-10806378096778 registered 29 Oct 2026 Active
  • FDA 510(k) K143394 decided 23 Jan 2015 Active
  • FDA GUDID UDI-DI 10806378096778 listed 24 Oct 2015 Listed

Timeline

3 dated events

  1. Cleared FDA 510(k) K143394
  2. Listed FDA GUDID 10806378096778
  3. Registered EUDAMED B-10806378096778

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD Active
  • United States FDA 510(k) Active

Specification

EUDAMED · GUDID

Trade name
Acumed
Generic name
Orthopaedic bone screw (non-sliding)
Device name
Peg
Model / reference
3014-23036
Primary DI / UDI-DI
10806378096778
Basic UDI-DI
B-10806378096778
510(k) Number
FDA product code
HRS
EMDN code
L091099 Osteosynthesis instruments, reusable - other
GMDN term
Orthopaedic bone screw (non-sliding)
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
888.3030
EU registration type
Legacy device (under a directive)
EU market of registration
Spain
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIa
GUDID
Class II
ImplantableEUDAMED
No
GUDID
Yes

Device class is stated on each registry's own scale: Class IIa in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Orthopaedic bone screw (non-sliding)

Cleared under the same submission (K143394)

and 8 more cleared under K143394

Similar devices in this category

Other devices filed under OSTEOSYNTHESIS INSTRUMENTS, REUSABLE - OTHER.

Other devices from Acumed LLC

See all devices from Acumed LLC →

Properties

  • Sterilise before use
  • Single use
  • Implantable NoEUDAMEDYesGUDID
  • Reusable
  • Prescription use
  • Lot / batch number
Other properties (19, all answered No)