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

Joint, Temporomandibular, Implant

21 CFR 872.3940 / Dental
FDA source (opens on fda.gov)

LZD is the FDA product code for Joint, Temporomandibular, Implant, a class III device type, regulated under 21 CFR 872.3940. FDA's definition for this code reads: "Call for PMAs to be filed by 3/30/99 per 63 FR 71746 on 12/30/98 - Indicated for reconstruction of the temporomandibular joint". As of , FDA records hold no 510(k) clearances under this code and 20 recalls.

Classification record

Product code
LZD
Device name
Joint, Temporomandibular, Implant
FDA definition
Call for PMAs to be filed by 3/30/99 per 63 FR 71746 on 12/30/98 - Indicated for reconstruction of the temporomandibular joint.
Regulation
21 CFR 872.3940
Device class
Class III
Review panel
Dental
Submission type
PMA
Implant
Yes
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
0
Ingested recalls
20

Companies listing this code with FDA

Companies whose registered establishments list this code