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Deknatel IPN025275

by Teleflex Incorporated 2 variants

Deknatel IPN025275 (RC-1387) is a Class II device made by Teleflex Incorporated, listed in FDA GUDID since 24 Mar 2017 (UDI-DI 14026704559678), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number14026704559678 UDI-DI Date24 Mar 2017ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Deknatel
Generic name
Silk suture
Model / Ref / Catalog
IPN025275, RC-1387
Primary DI / UDI-DI
14026704559678
FDA product code
OVN
GMDN term
Silk suture
Device class
Class II
Regulation number
878.4830
GUDID distribution status
In Commercial Distribution
MRI safety
MR Safe
Size
Length — 45 Centimeter

Related devices

Category: Silk suture

Similar devices

Also classified as Silk suture.

Similar devices in this category

Other devices filed under Silk suture.

Other devices from Teleflex Incorporated

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    Class II

See all devices from Teleflex Incorporated →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (7, all answered No)