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

Instrument, Cast Application/Removal, Manual

21 CFR 888.5980 / Orthopedic
FDA source (opens on fda.gov)

LGG is the FDA product code for Instrument, Cast Application/Removal, Manual, a class I device type, regulated under 21 CFR 888.5980. As of , FDA records hold 3 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
LGG
Device name
Instrument, Cast Application/Removal, Manual
Regulation
21 CFR 888.5980
Device class
Class I
Review panel
Orthopedic
Submission type
510(k) exempt
Implant
No
Life sustaining or supporting
No
GMP exempt
Yes
Third party review eligible
No
Ingested clearances
3
Ingested recalls
0

Clearances, product code LGG

By decision year
3 clearances under product code LGG with a decision year between 1984 and 1987, 1984 the highest year at 1.
Show the numbers
510(k) clearances under FDA product code LGG by decision year
YearClearances
19841
19851
19871

Applicants with the most clearances

Product code LGG
Applicants holding the most 510(k) clearances under product code LGG
ApplicantClearances
Artiberia1
Buckman Co., Inc.1
Mizuho Orthopedic Systems Inc1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 100 companies shown, in name order