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Activa BioActive-Base/Liner Sample SVB

by Pulpdent Corporation

Activa BioActive-Base/Liner Sample SVB is a Class II device made by Pulpdent Corporation, listed in FDA GUDID since 10 Aug 2018 (UDI-DI D701SVB2), 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 NumberD701SVB2 UDI-DI Date10 Aug 2018ListedStatusListed 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  • Withdrawn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
Activa BioActive-Base/Liner Sample
Generic name
Dental composite resin
Model / reference
SVB
Primary DI / UDI-DI
D701SVB2
FDA product code
EJK
GMDN term
Dental composite resin
Device class
Class II
Regulation number
872.3250
GUDID distribution status
In Commercial Distribution
Size
Total Volume — 0.6 Milliliter

Related devices

Category: Dental composite resin

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Other devices filed under Dental composite resin.

Other devices from Pulpdent Corporation

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Properties

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