Not currently registered with FDA under this name

J. Aderer, Inc.

Mchenry, IL, United States. Named as applicant on 23 dental 510(k) clearances between 1981 and 1982. No establishment is registered with FDA under this exact name today.

Device types listed: 0
Brands and models: 0
510(k) clearances: 231981–1982
Markets registered in: 1United States
Establishments: 0—

510(k) clearances per year, 1980–2026

510(k) clearances

Clearances on which FDA names J. Aderer, Inc. as the applicant.

Decided	510(k)	Device	Device type
26 Oct 1982	K822957	PURCAST	EJH Base Metal Alloy
26 Oct 1982	K822956	G CAST	EJT Gold-Based Noble Metal Alloy
13 Jul 1982	K821798	82 ALLOY	EJS Alloy Other Noble Metal
6 Jul 1982	K821832	DEGUCAST U	EJS Alloy Other Noble Metal
14 Jun 1982	K821590	PORS-ON	EJS Alloy Other Noble Metal
14 Jun 1982	K821572	DUALLOR 'R'	EJS Alloy Other Noble Metal
9 Jun 1982	K821521	STABILOR NF	EJT Gold-Based Noble Metal Alloy
9 Jun 1982	K821446	DEGUDENT 14	EJT Gold-Based Noble Metal Alloy
9 Jun 1982	K821407	DEVA M	EJS Alloy Other Noble Metal
4 Jun 1982	K821613	E.G. BRIDGE GOLD	EJT Gold-Based Noble Metal Alloy
28 May 1982	K821299	CER-MATE	EJS Alloy Other Noble Metal
10 May 1982	K821022	PRECIOUS METAL ALLOYS	EJS Alloy Other Noble Metal
5 May 1982	K820955	BOND-ON	EJS Alloy Other Noble Metal
2 Mar 1982	K820318	SPECIAL WHITE	EJT Gold-Based Noble Metal Alloy
7 Jan 1982	K813418	INZOMA NP	EJS Alloy Other Noble Metal
7 Jan 1982	K813417	INZOMA P	EJT Gold-Based Noble Metal Alloy
2 Oct 1981	K811867	SR-ALGICAP	ELW Impression Material
15 Jul 1981	K811665	SR-ISOCETTE	ELK Backing and Facing Artificial Teeth
14 Apr 1981	K810687	SR-IVOCAP	EBI Rebasing Repairing Relining Denture Resin
14 Apr 1981	K810686	SR-IVOLEN	EBH Resin Impression Tray Material
14 Apr 1981	K810523	SR-IVOSEAL	ELW Impression Material
17 Mar 1981	K810525	SR-IVOTRAY UNIVERSAL	EHY Preformed Impression Tray
17 Mar 1981	K810524	SR-IVOTRAY SPECIAL	EHY Preformed Impression Tray

Sources

FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record of the most recent filing, which can be a US agent.