← Back to manufacturers

Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

Midmark Corporation

United States·US-MF-000002581

Last updated September 17, 2026

About

Midmark is a global manufacturer and supplier of healthcare products, equipment and diagnostic software for medical, veterinary, and dental markets.

From the manufacturer's own website. Source

Information

Country
United States
Address
60, Vista Drive, Versailles, United States
Website
www.midmark.com
LinkedIn
linkedin.com/company/midmark-corporation/posts
Facebook
facebook.com/MidmarkCorporation
Email
[email protected]
Phone
—
PRRC Contact
Adam Clutter
EUDAMED SRN
US-MF-000002581
FDA FEI Number
1523530
DUNS Number
—

Catalogue (1527)

Page 27 of 31
DeviceModel / ReferenceRegistriesClassStatus
Midmark OptiMax Digital Sensor System XSDN-04
FDA UDI
Class IIActive
Midmark PREVA IntraOral Dental X-ray System DCDM-W0A/H/S1
FDA UDI
Class IIActive
Preva, 56" Reach, Uk PE7015-UK
FDA UDI
Class IIActive
Midmark PREVA 2.0 IntraOral Dental X-ray System DCD5DE‐W1Y/H
FDA UDI
Class IIActive
Midmark PREVA IntraOral Dental X-ray System DCDM-W0B/H/S1
FDA UDI
Class IIActive
Midmark ClearVision Digital Sensor System XSDS-0B/L
FDA UDI
Class IIActive
Midmark PREVA IntraOral Dental X-ray System P7015-P
FDA UDI
Class IIActive
Midmark Progeny Imaging Software 45-A0023
FDA UDI
Class IIActive
Pan system with ceph sensor, export V5150
FDA UDI
Class IIActive
Preva, 76" Reach, Uk PE7017-UK
FDA UDI
Class IIActive
Progeny Vantage Panoramic X-Ray System K091866
FDA 510(k)
Class IIActive
Surgi-Med Table Model 485-Lt K841505
FDA 510(k)
N/AActive
Midmark M3 Ultrafast Automatic Sterilizer K090670
FDA 510(k)
Class IIActive
Multiple, Model #17 K820823
FDA 510(k)
Class IActive
Ritter Model 158 And 159 Exam Lights K932719
FDA 510(k)
Class IActive
Midmark and Ritter M9 and M11 UltraClave® Automatic Sterilizers and Ritter M9D AutoClave® Automatic Sterilizer K163337
FDA 510(k)
Class IIActive
Midmark M4*9 Easyclave Steam Sterilizer K992744
FDA 510(k)
Class IIActive
Midmark M9 Ultraclave Steam Sterilizer K023348
FDA 510(k)
Class IIActive
Elevance K120239
FDA 510(k)
Class IActive
Multiple, Ent Chair #418 K822530
FDA 510(k)
Class IActive
Midmark Smart M9® Sterilizer, Midmark Smart M11® Sterilizer K233026
FDA 510(k)
Class IIActive
Power Podiatry Chair/Table #414, #416 & #417 K894017
FDA 510(k)
Class IActive
Lithotomy Chair #415 K831385
FDA 510(k)
Class IActive
Power Examination Table Model # 405 K894144
FDA 510(k)
Class IActive
Midmark Extraoral Imaging System (EOIS) K201667
FDA 510(k)
Class IIActive
712 Plastic Surgery Table & Accesories K915141
FDA 510(k)
Class IActive
Rittermodel 75 Evolution Univ Pow Exam Table/Acces K926463
FDA 510(k)
Class IActive
X-Ray Collimating Devices K810598
FDA 510(k)
Class IIActive
Midmark Dental Delivery System K251626
FDA 510(k)
Class IActive
Midmark Magnum General Surgical Table K934744
FDA 510(k)
Class IActive
Model #m9 Ultraclave Steam Sterilizer K911322
FDA 510(k)
Class IIActive
IQvitals Zone K161909
FDA 510(k)
Class IIActive
Model 561 C-Arm Procedures Stretcher K923730
FDA 510(k)
Class IIActive
Midmark M-11 Ultraclave Steam Sterilizer K936181
FDA 510(k)
Class IIActive
Clearvision K112380
FDA 510(k)
Class IIActive
Power Examination Table Model # 411 K894134
FDA 510(k)
Class IActive
Multiple, Ent Cabinet #448 K822531
FDA 510(k)
Class IActive
Modification Of: Midmark M-11 Ultraclave Steam Sterilizer K990189
FDA 510(k)
Class IIActive
#491 Power Otolaryngoly Ch/#498 Proced Ctr & Acces K910781
FDA 510(k)
Class IActive
Midmark Surgical Lighting Systems K930686
FDA 510(k)
Class IIActive
Model #510/515 General Transport Stretcher K895016
FDA 510(k)
Class IActive
Vantage Model V5000, V5100, V5000c, V5100c K122643
FDA 510(k)
Class IIActive
Three Models Of Tables, Stools, & Lights K811190
FDA 510(k)
Class IActive
Model 500 Pediatric Stretcher/Crib K852422
FDA 510(k)
Class IIActive
Model #527 Ophthalmic Stretcher K904011
FDA 510(k)
Class IIActive
Model #m8 Electronic Sterilizer K900432
FDA 510(k)
Class IIActive
Model #535 Pacu Stretcher/Bed & #530 Ed/Trauma Str K894335
FDA 510(k)
Class IIActive
Midmark Procenter Instrument Delivery System K003090
FDA 510(k)
Class IActive
Midmark 9A500001-863
EUDAMEDFDA UDI
Class IActive
Midmark 9A496001-870
EUDAMEDFDA UDI
Class IActive

Related Companies

Authorised Representatives

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Recalls (1)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

DateRecall No.ClassStatusReason
Mar 5, 2003Z-0704-03—terminated

The pressure relief valve may fail to open properly.