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DemeSILK SK13602W

by DemeTECH Corp

Ref SK13602W

DemeSILK SK13602W is a device classified as Class IIb in the EU and Class II in the US made by DemeTECH Corp, registered in EUDAMED on 9 Jul 2026 (Basic UDI-DI B-10652927306160), cleared under FDA 510(k) K023029 on 25 Nov 2002 and listed in FDA GUDID since 19 Jun 2019 (UDI-DI 10652927306160), active as of 24 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 24 Oct 2026

Documents

None linked in EUDAMED

A group certificate may exist

510(k) K023029

FDA submission, from GUDID

Trust

Unverified

Source EUDAMED, GUDID, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-10652927306160 Basic UDI-DI 10652927306160UDI-DIDate9 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10652927306160 UDI-DI Date19 Jun 2019ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE GUDID from GUDID Substantially Equivalent · Traditional NumberK023029 Date25 Nov 2002DecidedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI B-10652927306160 registered 9 Jul 2026 Active
  • FDA 510(k) K023029 decided 25 Nov 2002 Active
  • FDA GUDID UDI-DI 10652927306160 listed 19 Jun 2019 Listed

Timeline

3 dated events

  1. Cleared FDA 510(k) K023029
  2. Listed FDA GUDID 10652927306160
  3. Registered EUDAMED B-10652927306160

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  • Withdrawn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
DemeSILK
Generic name
Silk suture
Model / reference
SK13602W
Primary DI / UDI-DI
10652927306160
Basic UDI-DI
B-10652927306160
510(k) Number
FDA product code
GAP
EMDN code
H010202020302 Silk without needle
GMDN term
Silk suture
Device class
Class IIb EUDAMED
Class II GUDID
Regulation number
878.5030
EU registration type
Legacy device (under a directive)
EU market of registration
Greece
GUDID distribution status
In Commercial Distribution

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: Silk suture

Cleared under the same submission (K023029)

and 8 more cleared under K023029

Similar devices in this category

Other devices filed under SILK.

Other devices from DemeTECH Corp

See all devices from DemeTECH Corp →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (17, all answered No)