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Conmed C2621

by Conmed Corporation

Ref C2621

Conmed C2621 is a device classified as Class IIb in the EU and Class II in the US made by Conmed Corporation, registered in EUDAMED on 17 Jun 2026 (Basic UDI-DI B-10845854015698), cleared under FDA 510(k) K954682 on 9 Feb 1996 and listed in FDA GUDID since 10 Dec 2015 (UDI-DI 10845854015698), active as of 25 Oct 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 25 Oct 2026

Documents

None linked in EUDAMED

A group certificate may exist

510(k) K954682

FDA submission, from GUDID

Trust

Unverified

Source EUDAMED, GUDID, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-10845854015698 Basic UDI-DI 10845854015698UDI-DIDate17 Jun 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10845854015698 UDI-DI Date10 Dec 2015ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SN GUDID from GUDID Traditional NumberK954682 Date9 Feb 1996DecidedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI B-10845854015698 registered 17 Jun 2026 Active
  • FDA 510(k) K954682 decided 9 Feb 1996 Active
  • FDA GUDID UDI-DI 10845854015698 listed 10 Dec 2015 Listed

Timeline

3 dated events

  1. Cleared FDA 510(k) K954682
  2. Listed FDA GUDID 10845854015698
  3. Registered EUDAMED B-10845854015698

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  • Withdrawn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
Conmed
Generic name
Implantable bone washer
Device name
Orthopedic, Implant, Non-absorbable, Washer, Titanium, Knee and Shoulder
Model / Ref / Catalog
C2621
Primary DI / UDI-DI
10845854015698
Basic UDI-DI
B-10845854015698
510(k) Number
FDA product code
HTN
EMDN code
P09120699 Bone fixation screws, tendon and ligament synthesis screws - other
GMDN term
Implantable bone washer
Device class
Class IIb EUDAMED
Class II GUDID
Regulation number
888.3030
EU registration type
Legacy device (under a directive)
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution
Size
Outer Diameter — 17 Millimeter

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIb
GUDID
Class II

Device class is stated on each registry's own scale: Class IIb 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: Implantable bone washer

Cleared under the same submission (K954682)

and 8 more cleared under K954682

Similar devices in this category

Other devices filed under BONE FIXATION SCREWS, TENDON AND LIGAMENT SYNTHESIS SCREWS - OTHER.

Other devices from Conmed Corporation

See all devices from Conmed Corporation →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (19, all answered No)