510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K924376Substantially Equivalent

Root Canal Post

The Thera Group, Westford MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K924376 is the FDA 510(k) clearance record for ROOT CANAL POST, a class I device, cleared for The Thera Group on under FDA product code EBL (Pin, Retentive And Splinting, And Accessory Instruments). FDA records list one 510(k) clearance for The Thera Group. As of , FDA records show no recalls naming K924376.

Clearance record

Decision date
Received
(451 days to decision)
Product code
EBL Pin, Retentive And Splinting, And Accessory Instruments
Regulation
21 CFR 872.3740
Device class
Class I
Review panel
Dental
Applicant
The Thera Group 7-B Old Colony Dr., Westford MA
510(k) summary
Statement
Third party review
No

Clearances, product code EBL

Trailing 12 months

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

FDA records show no clearances under product code EBL in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code EBL, 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