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Conmed C2610

by Conmed Corporation

Conmed C2610 is a Class II device made by Conmed Corporation, cleared under FDA 510(k) K954682 on 9 Feb 1996 and listed in FDA GUDID since 26 Oct 2015 (UDI-DI 20845854019389), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

510(k) K954682

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number20845854019389 UDI-DI Date26 Oct 2015ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SN from GUDID Traditional NumberK954682 Date9 Feb 1996DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K954682 decided 9 Feb 1996 Active
  • FDA GUDID UDI-DI 20845854019389 listed 26 Oct 2015 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K954682
  2. Listed FDA GUDID 20845854019389

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Conmed
Generic name
Tendon/ligament bone anchor, non-bioabsorbable
Model / Ref / Catalog
C2610
Primary DI / UDI-DI
20845854019389
510(k) Number
FDA product code
HTN
GMDN term
Tendon/ligament bone anchor, non-bioabsorbable
Device class
Class II
Regulation number
888.3030
GUDID distribution status
In Commercial Distribution
Size
Length — 25 Millimeter
Outer Diameter — 6.5 Millimeter

Similar devices in this category

Other devices filed under Tendon/ligament bone anchor, non-bioabsorbable.

Other devices from Conmed Corporation

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Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)