FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Nexus Universal, Nexus Universal Chroma

K Number: K151332 · Decision Aug 17, 2015
Classifications
1
FEI Numbers
144
Registration Numbers
144
Same Product Code
504
Applicant Total
15
Review Days
90

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
Nexus Universal, Nexus Universal Chroma
K Number
K151332
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
872.3275
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sybron Dental Specialties
Date Received
May 19, 2015
Decision Date
August 17, 2015
Product Code
EMA
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
EMA Cement, Dental

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (EMA), ordered by most recent decision date.

View all

Other Clearances by Sybron Dental Specialties

K Number Device Name
K182826 Ormco Spark Aligner System
K162063 Steri-Cassette and Steri-Cage Sterilization Packaging System
K160097 Image Fast Set, Image Regular Set
K153067 Tubli-Seal, Tubli-Seal EWT,Tubli-Seal Xpress, Tubli-Seal EWT Xpress
K152956 Pulp Canal Sealer, Pulp Canal Sealer EWT
K152959 Sealapex tubes, Sealapex bulk package, Sealapex Xpress dual-barrel syringes
K151526 Zone, ZoneFree, Zone A1
K150559 Life Fast Set, Life Regular Set
K143209 SonicFill 2
K130869 TAKE 1 ADVANCE
Search all 15 clearances from Sybron Dental Specialties →