Manufacturer Intelligence · Based on 18,495 FDA 510(k) records · 70 countries

FDA 510(k) Medical Device Manufacturers - United States

U.S. medical device manufacturers ranked by FDA 510(k) submission volume. This is not a curated directory - rankings reflect real submission activity extracted from FDA accessdata.gov records.

  • Compare manufacturers by FDA 510(k) submission activity
  • Identify clearance rates, active panels and years of FDA activity
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4329
Manufacturers
United States
Country

United States Manufacturers

1–50 of 4,329
# Manufacturer Submissions Cleared Active panels Country
1 152 100%
CV RA
US
2 111 100%
OR SU
US
3 93 99%
AN CV EN +6
US
4 65 100%
EN RA SU
US
5 63 100%
AN CH HE +4
US
6 63 100%
OR SU
US
7 58 100%
CH HE IM +1
US
8 57 100%
CV GU HO +1
US
9
Medtronic, Inc.
Mounds View
54 100%
CV NE OR +2
US
10
Abbott Medical
S,Mta Clara
53 100%
CV NE
US
11 50 100%
CV GU RA +1
US
12 46 100%
RA
US
13
Roche Diagnostics
Indianapolos
44 100%
CH HE IM +2
US
14 43 100%
NE OR RA
US
15 41 100%
NE OR RA +1
US
16 41 100%
OR
US
17 40 100%
OR
US
18 36 97%
CH IM MI +1
US
19 35 97%
AN GU HO +4
US
20 34 100%
CV NE PM
US
21 34 100%
OR SU
US
22 34 97%
CV GU HO +1
US
23 33 100%
CV GU
US
24 33 100%
OR
US
25 33 100%
DE GU HO +1
US
26 33 100%
NE OR SU
US
27
Covidien, LLC
Mansfield
33 97%
AN EN GU +2
US
28 32 100%
CV NE SU
US
29
Life Spine, Inc.
Hoffman Estates
32 100%
OR
US
30 31 100%
AN CV EN +6
US
31 31 100%
AN EN GU +3
US
32
3M Company
White City
30 97%
CV HO SU
US
33 30 100%
IM MI
US
34 29 100%
AN CV HO +3
US
35 27 100%
DE GU NE +2
US
36 27 100%
DE HO
US
37 26 96%
HE MI RA
US
38 26 100%
OR
US
39 25 100%
OR
US
40 25 92%
AN CV HO +1
US
41
Covidien
North Haven
25 100%
AN HO SU
US
42 25 100%
OR
US
43 25 100%
CV HO
US
44 24 100%
RA
US
45
Stryker
Portage
24 100%
DE NE OR +1
US
46 24 100%
EN GU SU
US
47 23 100%
EN GU HO +3
US
48 22 100%
CH TX
US
49 22 95%
MI OB PA +1
US
50 22 100%
HO NE OB +2
US

About This FDA 510(k) Manufacturer Database

Data Source and Methodology

Rankings are based on the total number of published FDA 510(k) submissions per manufacturer in the 510k Database dataset, derived from FDA 510(k) public files. This is not a curated or paid listing - manufacturer rankings reflect real regulatory activity.

Used by regulatory affairs teams and medtech consultants to benchmark manufacturer activity, identify predicate device candidates, and analyze competitive positioning across FDA review panels.