Is this your brand? Sign in to claim ownership.

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 21 of 31

Device	Model / Reference	Registries	Class	Status
Midmark	9A386001-814	FDA UDI	Class I	Active
Ritter	203-012	FDA UDI	Class I	Active
Midmark	P21SC/CV3	FDA UDI	Class I	Active
Midmark	9A378001-862	FDA UDI	Class I	Active
Ritter	203-013	FDA UDI	Class I	Active
Midmark	P21SC/CV3R	FDA UDI	Class I	Active
Midmark	204 Manual Examination Table	FDA UDI	Class I	Unknown
Midmark	9A739001-855	FDA UDI	Class I	Active
Midmark PREVA IntraOral Dental X-ray System	DCD8DE-W2Y/H/S2	FDA UDI	Class II	Active
Midmark PREVA IntraOral Dental X-ray System	DCD8-G2N/SB	FDA UDI	Class II	Active
Midmark	P52SC/G5	FDA UDI	Class I	Active
Midmark	9A390001-858	FDA UDI	Class I	Active
Midmark Intraoral Digital Sensor	XSDN-06	FDA UDI	Class II	Active
Ritter	253-013	FDA UDI	Class I	Active
Midmark	G3	FDA UDI	Class I	Active
Midmark	P22	FDA UDI	Class I	Active
Midmark	DCVM-G0X/H/S4/L	FDA UDI	Class II	Active
Midmark PREVA IntraOral Dental X-ray System	DCD5DE‐W2X/H/S2	FDA UDI	Class II	Active
Midmark PREVA 2.0 IntraOral Dental X-ray System	DCD5DE‐W2X/H	FDA UDI	Class II	Active
Midmark Extraoral Imaging System (EOIS)	60-A1041	FDA UDI	Class II	Active
Midmark	CBML-L	FDA UDI	Class I	Active
Ritter	225-002	FDA UDI	Class I	Active
Midmark	9A390001-845	FDA UDI	Class I	Active
Ritter	255-001	FDA UDI	Class I	Active
Midmark	9A684001-813	FDA UDI	Class I	Active
Midmark	253-006	FDA UDI	Class I	Active
Midmark	9A378001-843	FDA UDI	Class I	Active
Midmark Extraoral Imaging System (EOIS)	60-A0012	FDA UDI	Class II	Active
Midmark	153908-002	FDA UDI	Class I	Active
Midmark	9A739001-864	FDA UDI	Class I	Active
Midmark	9A394001-852	FDA UDI	Class I	Active
Midmark VETPRO IntraOral Dental X-ray System	DCV7-G2A/H/S3	FDA UDI	Class II	Active
Midmark PREVA 2.0 IntraOral Dental X-ray System	DCDM-G0A/H	FDA UDI	Class II	Active
Midmark	9A382001-843	FDA UDI	Class I	Active
Midmark	9A684001-813	FDA UDI	Class I	Active
Ritter	9A51001-865	FDA UDI	Class I	Active
Midmark	DCD8-G2Z	FDA UDI	Class II	Active
Preva 2.0 Mobile Wht Retrofit	XSAM‐W0	FDA UDI	Class II	Active
Midmark	9A684001-813	FDA UDI	Class I	Active
Midmark	DCD8-G2Z/SB	FDA UDI	Class II	Active
Midmark Intraoral Digital Sensor	XSVS-06	FDA UDI	Class II	Active
Midmark	9A386001-862	FDA UDI	Class I	Active
Midmark	9A684001-813	FDA UDI	Class I	Active
Midmark	DCV5-G1X/H/SC	FDA UDI	Class II	Active
Midmark PREVA IntraOral Dental X-ray System	DCD6-W2M/H/S1	FDA UDI	Class II	Active
Midmark	DCD6-G1Z/S2	FDA UDI	Class II	Active
Midmark PREVA IntraOral Dental X-ray System	30-A2201	FDA UDI	Class II	Active
Preva Export Mobile System, Deutsch	PE7017DM	FDA UDI	Class II	Active
Midmark	QC1-01	FDA UDI	Class I	Active
Midmark	DCV5-G1A/H/SB	FDA UDI	Class II	Active

Related Companies

Authorised Representatives

CEpartner4U NL

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.

Date	Recall No.	Class	Status	Reason
Mar 5, 2003	Z-0704-03	—	terminated	The pressure relief valve may fail to open properly.