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Acumed Co-S2308-S

by Acumed LLC

Ref CO-S2308-S

Acumed Co-S2308-S is a device classified as Class IIb in the EU and Class I in the US made by Acumed LLC, registered in EUDAMED on 26 Oct 2026 (Basic UDI-DI B-10806378061943), cleared under FDA 510(k) K120903 on 13 Jul 2012 and listed in FDA GUDID since 24 Oct 2015 (UDI-DI 10806378061943), 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) K120903

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-10806378061943 Basic UDI-DI 10806378061943UDI-DIDate26 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10806378061943 UDI-DI Date24 Oct 2015ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE GUDID from GUDID Substantially Equivalent · Special NumberK120903 Date13 Jul 2012DecidedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI B-10806378061943 registered 26 Oct 2026 Active
  • FDA 510(k) K120903 decided 13 Jul 2012 Active
  • FDA GUDID UDI-DI 10806378061943 listed 24 Oct 2015 Listed

Timeline

3 dated events

  1. Cleared FDA 510(k) K120903
  2. Listed FDA GUDID 10806378061943
  3. Registered EUDAMED B-10806378061943

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  • Withdrawn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-bioabsorbable, sterile
Device name
Trial
Model / reference
CO-S2308-S
Primary DI / UDI-DI
10806378061943
Basic UDI-DI
B-10806378061943
510(k) Number
FDA product code
LXH
EMDN code
L091099 Osteosynthesis instruments, reusable - other
GMDN term
Orthopaedic bone screw, non-bioabsorbable, sterile
Device class
Class IIb EUDAMED
Class I GUDID
Regulation number
888.4540
EU registration type
Legacy device (under a directive)
EU market of registration
Spain
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 3 fields differ

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIb
GUDID
Class I
Supplied sterileEUDAMED
No
GUDID
Yes
Sterilise before useEUDAMED
Yes
GUDID
No

Registry differences

EUDAMED and FDA GUDID describe the same product (same UDI-DI) and state different values:

  • Supplied sterile UDI-DI 10806378061943: EUDAMED states No, FDA GUDID states Yes.
  • Sterilise before use UDI-DI 10806378061943: EUDAMED states Yes, FDA GUDID states No.

Device class is stated on each registry's own scale: Class IIb in the EU (EUDAMED), Class I 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-bioabsorbable, sterile

Cleared under the same submission (K120903)

and 8 more cleared under K120903

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

  • Supplied sterile NoEUDAMEDYesGUDID
  • Sterilise before use YesEUDAMEDNoGUDID
  • Single use
  • Prescription use
  • Lot / batch number
Other properties (20, all answered No)