510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K852894Unknown

Ormco Transmandibular Implant

Ormco Corp., Glendora CA / Traditional, Unknown
FDA source (opens on fda.gov)

K852894 is the FDA 510(k) clearance record for ORMCO TRANSMANDIBULAR IMPLANT, a class II device, cleared for Ormco Corp. on under FDA product code MDL (Implant, Transmandibular). FDA records list 27 510(k) clearances for Ormco Corp., from to . As of , FDA records show no recalls naming K852894.

Clearance record

Decision date
Received
(51 days to decision)
Product code
MDL Implant, Transmandibular
Regulation
21 CFR 872.4760
Device class
Class II
Review panel
Dental
Applicant
Ormco Corp. 1332 S. Lone Hill Ave., Glendora CA
Third party review
No

Clearances, product code MDL

Trailing 12 months

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

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