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Immediate Placement Device IPIP

by Ebi, Inc.

Immediate Placement Device IPIP is a Class I device made by Ebi, Inc., listed in FDA GUDID since 23 Feb 2026 (UDI-DI 08809823979157), registry data as of 12 Nov 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 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08809823979157 UDI-DI Date23 Feb 2026ListedStatusListed 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  • Withdrawn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
Immediate Placement Device
Generic name
Dental implant system
Model / reference
IPIP
Primary DI / UDI-DI
08809823979157
FDA product code
NDP
GMDN term
Dental implant system
Device class
Class I
Regulation number
872.3980
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code NDP (Accessories, Implant, Dental, Endosseous).

Other devices from Ebi, Inc.

See all devices from Ebi, Inc. →

Properties

  • Implantable
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)