Wallace A. Erickson & Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Wallace A. Erickson & Co. - FDA 510(k) Cleared Devices
32
Total
32
Cleared
0
Denied
Wallace A. Erickson & Co. has 32 FDA 510(k) cleared dental devices. Based in Mchenry, US.
Historical record: 32 cleared submissions from 1978 to 1999.
Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Wallace A. Erickson & Co.
32 devices
Cleared
Feb 26, 1999
ALPHA BOND DENTIN/ENAMEL BONDING AGENT, MODEL 213-000
Dental
70d
Cleared
Dec 06, 1996
ALPHA-DENT ROOT CANAL SEALER & FILLER
Dental
67d
Cleared
Jul 02, 1996
CENTRIX FLOFIL/CENTRIX FLOFIL WITH FLUORIDE
Dental
133d
Cleared
Mar 28, 1996
ALPHA-DENT HEMA DESENTIZER(748-000)/WITH FLUORIDE(747-000)
Dental
63d
Cleared
Mar 15, 1996
ALPHA-DENT COMPOSITE SURFACE SEALANT
Dental
59d
Cleared
Feb 21, 1996
ALPHA-DENT TEMPORARY CROWN AND BRIDGE MATERIAL
Dental
36d
Cleared
Jan 24, 1996
ALPHA-DENT COPAL CAVITY VARNISH
Dental
51d
Cleared
Dec 13, 1995
ALPHA-DENT ZINC OXIDE EUGENOL TEMPORARY CEMENT
Dental
36d
Cleared
Aug 29, 1994
ALPHA BOND-RITE II(TM) OR BOND-RITE II(TM) 2-PASTE ADHEV
Dental
80d
Cleared
Aug 23, 1994
ALPHA BOUND-RITE I NO-MIX ADHESIVE OR BOND-RITE I NO-MIX ADHESIVE
Dental
75d
Cleared
Aug 10, 1994
ALPHADENT LIGHT ACTIVATED ORTHODONTIC ADHESIVE BONDING SYSTEM WITH FLUORIDE
Dental
261d
Cleared
Jul 08, 1994
ALPHA-DENT C-R(R) HYBRID TYPE II COMPOSITE RESIN
Dental
25d