Skip to content

UNIFY PDO Surgical Sutures XXL-D430K60

by Applied Dental, Inc.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00814639026825 UDI-DI Date12 Nov 2025ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
UNIFY PDO Surgical Sutures
Generic Name
Nylon suture, non-bioabsorbable, monofilament
Model / Ref / Catalog
XXL-D430K60
Primary DI / UDI-DI
00814639026825
FDA Product Code
NEW
GMDN Term
Nylon suture, non-bioabsorbable, monofilament
Device Class
Class II
Regulation Number
878.4840
GUDID distribution status
In Commercial Distribution

Other devices from Applied Dental, Inc.

See all devices from Applied Dental, Inc. →

Properties

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

Other properties (9)

  • Implantable: No
  • 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