510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K912724Substantially Equivalent for Some Indications

Guidor(tm)

Procordia Oratech AB, Huddinge, Sweden, SE / Traditional, Substantially Equivalent for Some Indications
FDA source (opens on fda.gov)

K912724 is the FDA 510(k) clearance record for GUIDOR(TM), a class II device, cleared for Procordia Oratech AB on under FDA product code NPK (Barrier, Synthetic, Intraoral). FDA's definition for product code NPK reads: "A synthetic dental barrier is a synthetic material device, such as ptfe, intended to aid in guided tissue and/or bone regeneration procedures and to act as a stable barrier for the containment of bone graft materials". FDA records list one 510(k) clearance for Procordia Oratech AB. As of , FDA records show no recalls naming K912724.

Clearance record

Decision date
Received
(695 days to decision)
Product code
NPK Barrier, Synthetic, Intraoral
Regulation
21 CFR 872.3930
Device class
Class II
Review panel
Dental
Applicant
Procordia Oratech AB Novum, Huddinge, Sweden, SE
Third party review
No

Clearances, product code NPK

Trailing 12 months

FDA records hold no clearances under product code NPK in the trailing twelve months.

FDA records show no clearances under product code NPK in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code NPK, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260