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Imtec Case-7

by Park Dental Research Corp

Imtec Case-7 is a Class I device made by Park Dental Research Corp, listed in FDA GUDID since 19 Jun 2026 (UDI-DI D769CASE70), 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 NumberD769CASE70 UDI-DI Date19 Jun 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  • Withdrawn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
Imtec
Generic name
Surgical instrument/implant rack
Model / reference
CASE-7
Primary DI / UDI-DI
D769CASE70
FDA product code
NDP
GMDN term
Surgical instrument/implant rack
Device class
Class I
Regulation number
872.3980
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Similar devices

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

Other devices from Park Dental Research Corp

See all devices from Park Dental Research Corp →

Properties

  • Sterilise before use
  • Prescription use
  • Lot / batch number
Other properties (12, all answered No)