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Filasilk SLK60780DN

by Meril Endo Surgery Private Limited

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08904255218130 UDI-DI Date6 Mar 2019ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Filasilk
Generic Name
Silk suture
Model / Ref / Catalog
SLK60780DN
Primary DI / UDI-DI
08904255218130
510(k) Number
FDA Product Code
GAP
GMDN Term
Silk suture
Device Class
Class II
Regulation Number
878.5030
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Safe

Related devices

Category: Silk suture

Cleared under the same submission (K172149)

Show all (12)

Other devices from Meril Endo Surgery Private Limited

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Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (8)

  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No