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Monoswift L923

by Riverpoint Medical LLC

Monoswift L923 is a Class II device made by Riverpoint Medical LLC, listed in FDA GUDID since 28 Feb 2025 (UDI-DI 00840277408839), 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 Number00840277408839 UDI-DI Date28 Feb 2025ListedStatusListed 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  • Withdrawn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
Monoswift
Generic name
Polyester suture, bioabsorbable, monofilament, non-antimicrobial
Model / reference
L923
Primary DI / UDI-DI
00840277408839
FDA product code
GAM
GMDN term
Polyester suture, bioabsorbable, monofilament, non-antimicrobial
Device class
Class II
Regulation number
878.4493
GUDID distribution status
In Commercial Distribution

Related devices

Category: Polyester suture, bioabsorbable, monofilament, non-antimicrobial

Similar devices in this category

Other devices filed under Polyester suture, bioabsorbable, monofilament, non-antimicrobial.

Other devices from Riverpoint Medical LLC

See all devices from Riverpoint Medical LLC →

Properties

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