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510(k) K920784

ORTHODONTIC FACE BOW W/ INNER WIRE by Gac Intl., Inc. — Product Code DZB

K920784 is an FDA 510(k) premarket notification submitted by Gac Intl., Inc. for the device "ORTHODONTIC FACE BOW W/ INNER WIRE". The FDA issued a decision of Substantially Equivalent on March 20, 1992. The device falls under product code DZB (Headgear, Extraoral, Orthodontic), a Class II device regulated under 21 CFR 872.5500. Gac Intl., Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 20, 1992
Date Received
February 20, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Headgear, Extraoral, Orthodontic
Device Class
Class II
Regulation Number
872.5500
Review Panel
DE
Submission Type

Other clearances by Gac Intl., Inc.

  • K981036 — SMARTBOND (April 5, 1999)
  • K942826 — ORTHODONITC METAL REINFORCED PLASTIC BRACKET (December 14, 1994)
  • K933542 — MESIAL LOOP BAR (August 5, 1994)
  • K932825 — MICROARCH GOLD BRACKET (May 9, 1994)
  • K932319 — ORTHODONTIC ELASTOMER (September 20, 1993)
  • K932025 — ION-IMPLANTED NEO SENTALLOY (September 13, 1993)
  • K920905 — BIOFORCE WIRE (November 4, 1992)
  • K923029 — ORTHODONTIC STAINLESS STEEL BRACKET (September 28, 1992)
  • K920850 — GAC THUMB-SUCKING CONTROL APPLIANCE (August 24, 1992)
  • K852179 — CERAMIC ORTHODONIT APPLIANCE (August 20, 1985)

Other clearances for product code DZB

  • K202855 — Orthodontic Facemask (June 21, 2021)
  • K162543 — Reverse Pull Adjustable Facemask (August 28, 2017)
  • K111169 — PROTRACTION FACE MASK, REVERSE PULL FACE MASK MODEL KM-PVS, KM-PIS, KM-PVM, KM-P (October 3, 2011)
  • K103019 — KJ MASK (June 9, 2011)
  • K052553 — NITOM LOCKING FACEBOW (December 22, 2005)
  • K051751 — EQUA-PULL SAFETY RELEASE MODULE (July 22, 2005)
  • K041718 — KELES FACEMASK (October 15, 2004)
  • K032392 — MORALES PROTRACTION FACEMASK (October 22, 2003)
  • K000358 — MULTI ADJUSTABLE FACE MASK (June 9, 2000)
  • K993224 — T-GEAR, MODEL TG/400-700 (February 11, 2000)

FDA data resources