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

STEADY RESIN

K Number: K870908 · Decision Mar 19, 1987
Classifications
1
FEI Numbers
166
Registration Numbers
166
Same Product Code
329
Applicant Total
13
Review Days
14

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
STEADY RESIN
K Number
K870908
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.3760
Medical Specialty
Dental
Decision
Substantially Equivalent
Applicant
Great Lakes Orthodontics, Ltd.
Date Received
March 5, 1987
Decision Date
March 19, 1987
Product Code
EBI
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
EBI Resin, Denture, Relining, Repairing, Rebasing

Similar 510(k) Clearances

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

View all

Other Clearances by Great Lakes Orthodontics, Ltd.

K Number Device Name
K172765 Smart Moves Complete
K150702 Exceed Tx
K083479 BIOCRYL X
K041718 KELES FACEMASK
K040881 METACRYL
K033632 VARIFLEX
K922818 SNORE-NO-MORE
K925275 SOFT DENTURE RELINE MATERIAL ELASTOLINE
K861424 ADAPTABLE CLASS III MASK
K840805 ORAL SAFE
Search all 13 clearances from Great Lakes Orthodontics, Ltd. →