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Paul Banditt SVS31

by Terlain Enterprises, Inc.

Paul Banditt SVS31 is a Class I device made by Terlain Enterprises, Inc., listed in FDA GUDID since 11 Dec 2023 (UDI-DI D955SVS311), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberD955SVS311 UDI-DI Date11 Dec 2023ListedStatusListed 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  • Withdrawn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
Paul Banditt
Generic name
Periotome, reusable
Model / reference
SVS31
Primary DI / UDI-DI
D955SVS311
FDA product code
EMJ
GMDN term
Periotome, reusable
Device class
Class I
Regulation number
872.4565
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Periotome, reusable

Other devices from Terlain Enterprises, Inc.

See all devices from Terlain Enterprises, Inc. →

Properties

  • Sterilise before use
  • Premarket exempt
Other properties (13, all answered No)