Manufacturer Intelligence · Based on 55,089 FDA 510(k) records · 74 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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5511
Manufacturers
United States
Country

United States FDA 510(k) Overview

4585
Manufacturers
43,326
Submissions
99%
Clearance rate

Leading United States FDA 510(k) manufacturers include Abbott Laboratories, Siemens Medical Solutions USA, Inc., C.R. Bard, Inc. and 5508 others.

The United States represents the largest segment of the FDA 510(k) dataset by far, with 4,585 manufacturers and 43,326 submissions since 1976 — a 98.6% clearance rate across all submission types. U.S.-based manufacturers span every FDA review panel, from cardiovascular and orthopedic systems to software-based medical devices and in vitro diagnostics.

Active in FDA 510(k) submissions since 1976. Many United States manufacturers work with FDA regulatory consultants to support U.S. market entry.

FDA 510(k) United States Manufacturers

1–50 of 5,511
# Manufacturer Submissions Cleared Active panels Country
1 883 100%
AN CH CV +10
US
2 782 100%
AN CV DE +4
US
3 645 99%
AN CV EN +9
US
4 632 100%
AN CH CV +12
US
5 530 98%
CV DE EN +9
US
6 505 100%
AN CH CV +14
US
7 475 97%
AN CH CV +9
US
8
Syva Co.
Mchenry
448 100%
AN CH HE +3
US
9 441 95%
CV DE EN +9
US
10 432 100%
CV EN GU +8
US
11 411 96%
DE HO NE +3
US
12 376 95%
AN EN HO +6
US
13 373 87%
CV DE EN +7
US
14 362 100%
AN CV DE +9
US
15 350 99%
HO OR SU
US
16 343 100%
CH HE IM +2
US
17 340 100%
AN CH HE +6
US
18
3M Company
White City
331 98%
AN CH CV +12
US
19 321 100%
AN CH CV +5
US
20 321 100%
CH HE IM +2
US
21
Bio-Rad
Mchenry
319 100%
CH HE IM +3
US
22 315 100%
AN CH CV +8
US
23 303 79%
CV DE GU +6
US
24 302 96%
EN HO OR +1
US
25 296 100%
CH HE IM +2
US
26 288 100%
CH HE IM +2
US
27 288 100%
NE OR SU
US
28 281 100%
AN CH CV +6
US
29 280 100%
CH HE IM +3
US
30 279 100%
AN DE HO +4
US
31 278 100%
AN GU HO +4
US
32 270 100%
CH HE IM +2
US
33 264 100%
CH HE HO +4
US
34 254 100%
AN CV NE +3
US
35 253 100%
CH GU HE +5
US
36 251 100%
CH HE IM +1
US
37 238 100%
AN CH CV +9
US
38 238 100%
CH CV HE +4
US
39 232 100%
AN CV EN +7
US
40 231 100%
CH HE IM +3
US
41 230 100%
AN CH CV +5
US
42 218 92%
CV EN GU +6
US
43 217 100%
DE
US
44 211 97%
AN CV EN +6
US
45
Medtronic, Inc.
Mounds View
210 100%
AN CV EN +7
US
46
Aesculap, Inc.
Burlingame
207 97%
CV DE GU +5
US
47 207 99%
NE OR RA +1
US
48 206 100%
AN CH CV +9
US
49 206 89%
CH CV DE +9
US
50 205 98%
CV DE EN +6
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.