64 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Accessories, Soft Lens Products
FDA Pre-Market Approval
FDA Class 2
·SENSITIVE EYES CLEANING/DISINFECTING SOLUTION
Accessories, Soft Lens Products
FDA Pre-Market Approval
FDA Class 2
·SENSITIVE EYES CLEANING/DISINFECTING SOLUTION
Accessories, Soft Lens Products
FDA Pre-Market Approval
FDA Class 2
·BAUSCH & LOMB(R) RENU(R) MULTI-PURPOSE SOLUTION
Accessories, Soft Lens Products
FDA Pre-Market Approval
FDA Class 2
·BAUSCH & LOMB(R) RENU(R) MULTI-PURPOSE SOLUTION
Accessories, Soft Lens Products
FDA Pre-Market Approval
FDA Class 2
·SENSITIVE EYES CLEANING/DISINFECTING SOLUTION
Accessories, Soft Lens Products
FDA Pre-Market Approval
FDA Class 2
·BAUSCH & LOMB(R) RENU(R) MULTI-PURPOSE SOLUTION
Accessories, Soft Lens Products
FDA Pre-Market Approval
FDA Class 2
·BAUSCH & LOMB(R) RENU(R) MULTI-PURPOSE SOLUTION
Accessories, Soft Lens Products
FDA Pre-Market Approval
FDA Class 2
·SENSITIVE EYES CLEANING/DISINFECTING SOLUTION
Accessories, Soft Lens Products
FDA Pre-Market Approval
FDA Class 2
·SENSITIVE EYES CLEANING/DISINFECTING SOLUTION
N.A.
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR88600231·Max. 2. Molar band W-Fit left 23
Trimline
FDA UDI
ORMCO CORPORATION·00889989051643·UPPER RIGHT SECOND MOLAR TRIMLINE BAND SIZE 23
LEONE SPA
FDA UDI
LEONE SPA·08033707032052·WEB 1ST MOLAR BANDS n.LR 23
Shoreline ACS
FDA UDI
Seaspine Orthopedics Corporation·10889981127053·Drill Guide, Fixed
N.A.
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR88600230051·Max. 2. Molar band W-Fit left 23
N.A.
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR88600230501·Max. 2. Molar band W-Fit left 23
N.A.
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR88600230101·Max. 2. Molar band W-Fit left 23
COMPACT 2000 WATER SEAL CHEST DRAINAGE UNIT
FDA 510(k)
FDA Class 2
·General Hospital
Assay, Hybridization And/Or Nucleic Acid Amplification For Detection Of Hepatitis C Rna,Hepatitis C Virus
FDA Pre-Market Approval
FDA Class 2
·APTIMA HCV QUANT DX ASSAY
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·BRYAN CERVICAL DISC PROSTHESIS
BRYAN CERVICAL DISC SYSTEM
FDA Adverse Event
Injury
·Product code MJO·March 1, 2012