Home / 510(k) Clearances / K990367

510(k) K990367

PDQ AND PDQ-TI ABUTMENT by Vident — Product Code DZE

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 21, 1999
Date Received
February 5, 1999
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Implant, Endosseous, Root-Form
Device Class
Class II
Regulation Number
872.3640
Review Panel
DE
Submission Type

Other clearances by Vident

  • K063768 — TITANIUM SCALLOPED ABUTMENT (June 27, 2007)
  • K060441 — VITA VM 7, MODEL NX77 XXXX, NX78XXXX, NX79 XXXX; VITA VM 8, MODEL VX60 XXXX, VX6 (April 27, 2006)
  • K052710 — VITA VM7, MODEL NX77 XXXX, NX78XXXX, NX79 XXXX; VITA VM 8, MODEL VX60 XXXX, VX61 (January 13, 2006)
  • K052130 — VITA IN-CERAM 2000 AL CUBES FOR INLAB, MODELS AL20/AL40 (August 15, 2005)
  • K050362 — VITA PM 7 (20 GRAM BOTTLES), VITA PM 7 (50 GRAM BOTTLES) (March 15, 2005)
  • K022996 — VITA IN-CERAM YZ CUBES FOR CEREC (October 9, 2002)
  • K012473 — VIDENT HEXTOP, SYNOCTA IN-CERAM BLANK/COPING MANUFACTURED BY VIDENT (September 11, 2002)
  • K000597 — VITA RESPONSE (May 17, 2000)
  • K984198 — WIDE BODY ABUTMENTS (February 18, 1999)
  • K982664 — VITA TITANIUM PORCELAIN (August 2, 1998)

Other clearances for product code DZE

  • K252168 — Straumann® BLC Implants - Indication Widening (March 10, 2026)
  • K253493 — Dentis SQ-SL AXEL Fixture (March 4, 2026)
  • K252197 — Nobel Biocare S Series Implants (February 18, 2026)
  • K252286 — BIORES Dental Implant System (February 2, 2026)
  • K252585 — ZENEX Implant System_R-System (January 8, 2026)
  • K250476 — NizPlant Dental Implant System (December 23, 2025)
  • K252145 — GEN5™ and GEN5+™ 3.3mmD Dental Implants (December 23, 2025)
  • K251605 — DIMPLO Implant System (December 22, 2025)
  • K252090 — Pterygoid Indication for GM Helix Implants (December 12, 2025)
  • K251129 — S.I.N. Tapered Pro Conical Zygoma Implant System (November 7, 2025)