MDLClass II

Implant, Transmandibular

21 CFR 872.4760 / Dental

MDL is the FDA product code for Implant, Transmandibular, a class II device type, regulated under 21 CFR 872.4760. As of 2026-09-10, FDA records hold 2 510(k) clearances under this code, the most recent dated 1990-11-16, and no recalls.

Classification record

Product code: MDL
Device name: Implant, Transmandibular
Regulation: 21 CFR 872.4760
Device class: Class II
Review panel: Dental
Submission type: 510(k)
Implant: Yes
Life sustaining or supporting: No
GMP exempt: No
Third party review eligible: No
Ingested clearances: 2
Ingested recalls: 0

Clearances, product code MDL

By decision year

2 clearances under product code MDL with a decision year between 1985 and 1990, 1985 the highest year at 1.

Show the numbers

510(k) clearances under FDA product code MDL by decision year
Year	Clearances
1985	1
1990	1

Applicants with the most clearances

Product code MDL

Applicants holding the most 510(k) clearances under product code MDL
Applicant	Clearances
Interphase Implants, Inc.	1
Ormco Corp.	1

Companies listing this code with FDA

Companies whose registered establishments list this code

No registered establishment in MDM’s records lists product code MDL.

Recent clearances

Product code MDL

Recent recalls

Product code MDL

FDA records show no recalls under product code MDL.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device classification database, ingested from openFDA. The definition, regulation number, device class and review panel are FDA’s own fields, reproduced without editing.

MDM adds the counts: clearances by decision year, the applicants holding the most clearances under this code, recalls that name it, and the registered establishments that list it. Every count is computed from ingested records only.

Data as of 2026-10-05, the FDA export date for this dataset. Page last changed 2026-09-05. View this product code on fda.gov (opens on fda.gov)