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

Elevator, Surgical, General & Plastic Surgery

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

GEG is the FDA product code for Elevator, Surgical, General & Plastic Surgery, a class I device type, regulated under 21 CFR 878.4800. As of , FDA records hold 12 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
GEG
Device name
Elevator, Surgical, 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
12
Ingested recalls
0

Clearances, product code GEG

By decision year
12 clearances under product code GEG with a decision year between 1978 and 1989, 1989 the highest year at 5.
Show the numbers
510(k) clearances under FDA product code GEG by decision year
YearClearances
19781
19841
19861
19874
19895

Applicants with the most clearances

Product code GEG
Applicants holding the most 510(k) clearances under product code GEG
ApplicantClearances
Kinetic Medical Products3
Zinnanti Surgical Instruments, Inc.2
Buckman Co., Inc.1
Cedar Surgical, Inc.1
Imm Enterprises, Ltd.1
Micro-Aire Surgical Instruments, Inc.1
Military Engineering, Inc.1
Orthopedic Equipment Co., Inc.1
Mizuho Orthopedic Systems Inc1

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 216 companies shown, in name order