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MacImpress VP-9008-MI

by Surgimac LLC

MacImpress VP-9008-MI (VP9008MI) is a Class II device made by Surgimac LLC, listed in FDA GUDID since 6 Jul 2026 (UDI-DI D105VP9008MI4), 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 NumberD105VP9008MI4 UDI-DI Date6 Jul 2026ListedStatusListed 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  • Withdrawn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
MacImpress
Generic name
Dental articulation paste/solution
Model / Ref / Catalog
VP-9008-MI, VP9008MI
Primary DI / UDI-DI
D105VP9008MI4
FDA product code
ELW
GMDN term
Dental articulation paste/solution
Device class
Class II
Regulation number
872.3660
GUDID distribution status
In Commercial Distribution

Other devices from Surgimac LLC

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Properties

  • Single use
  • Contains latex
  • Expiration date
  • Manufacturing date
Other properties (11, all answered No)