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JBP V Line Edge 19Gx45mm 3LS19V41003GA

by Feeltech Co., Ltd.

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 Number18800145525913 UDI-DI Date25 Aug 2026ListedStatusListed 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  • Withdrawn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
JBP V Line Edge 19Gx45mm
Generic Name
Polyester suture, bioabsorbable, monofilament, non-antimicrobial
Model / Reference
3LS19V41003GA
Primary DI / UDI-DI
18800145525913
510(k) Number
FDA Product Code
NEW
GMDN Term
Polyester suture, bioabsorbable, monofilament, non-antimicrobial
Device Class
Class II
Regulation Number
878.4840
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K250107)

Show all (12)

Other devices from Feeltech Co., Ltd.

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Properties

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

Other properties (8)

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