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Expasyl 34619

by Kerr Corporation

Expasyl 34619 is a gingival retraction cord (FDA unclassified; FDA product code MVL, Cord, Retraction) made by Kerr Corporation, listed in FDA GUDID since 31 Aug 2016 (UDI-DI 10841396117098), 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 Number10841396117098 UDI-DI Date31 Aug 2016ListedStatusListed 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  • Withdrawn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
Expasyl
Generic name
Gingival retraction cord, medicated
Model / reference
34619
Primary DI / UDI-DI
10841396117098
FDA product code
MVL
GMDN term
Gingival retraction cord, medicated
Device class
U
GUDID distribution status
In Commercial Distribution
Size
Weight — 20 Gram

Similar devices

Other devices filed under FDA product code MVL (CORD, RETRACTION).

Other devices from Kerr Corporation

See all devices from Kerr Corporation →

Properties

  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)