510k
Database
Specialties
Anesthesiology
1348
Cardiovascular
4943
Chemistry
3701
Dental
2821
Ear, Nose, Throat
476
Gastroenterology & Urology
2540
General & Plastic Surgery
4286
General Hospital
3951
Hematology
889
Immunology
864
Medical Genetics
15
Microbiology
1944
Neurology
1921
Obstetrics & Gynecology
896
Ophthalmic
506
Orthopedic
8239
Pathology
187
Physical Medicine
978
Radiology
5193
Toxicology
1303
Categories
LLZ
System, Image Processing,...
758
HRS
Plate, Fixation, Bone
696
IYN
System, Imaging, Pulsed Doppler,...
609
GEI
Electrosurgical, Cutting &...
579
GEX
Powered Laser Surgical Instrument
526
JWH
Prosthesis, Knee,...
522
LZA
Polymer Patient Examination Glove
489
LNH
System, Nuclear Magnetic...
475
MAX
Intervertebral Fusion Device...
444
NKB
Thoracolumbosacral Pedicle Screw...
438
Browse all 339 categories →
Manufacturers
Search
Reports
Glossary
About
Search FDA 510(k) devices
Home
Manufacturers
US
Jmea Corporation
Medical Device Manufacturer
·
US , Rockville , MD
Jmea Corporation - FDA 510(k) Cleared Devices
1 submissions
·
1 cleared
·
Since 2008
1
Total
1
Cleared
0
Denied
FDA 510(k) Regulatory Record - Jmea Corporation
Orthopedic
✕
1
devices
1-1 of 1
Filters
Cleared
Aug 20, 2008
JMEA CANNULATED BONE SCREW SYSTEM
K080259
·
HWC
Orthopedic
·
202d
Filters
Filter by Specialty
All
1
Orthopedic
1