510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
FTXClass I

Mirror, General & Plastic Surgery

21 CFR 878.4800 / General, Plastic Surgery
FDA source (opens on fda.gov)

FTX is the FDA product code for Mirror, General & Plastic Surgery, a class I device type, regulated under 21 CFR 878.4800. As of , FDA records hold one 510(k) clearance under this code, the most recent dated , and no recalls.

Classification record

Product code
FTX
Device name
Mirror, General & Plastic Surgery
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
1
Ingested recalls
0

Clearances, product code FTX

By decision year
1 clearance under product code FTX with a decision year between 1987 and 1987, 1987 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code FTX by decision year
YearClearances
19871

Applicants with the most clearances

Product code FTX
Applicants holding the most 510(k) clearances under product code FTX
ApplicantClearances
Lifestream Int'L, Inc.1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 38 companies shown, in name order