Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

PONTALLOR 4 DENTAL ALLOY

K-Number: K870024 · 1987-03-11

ApplicantDegussa Dental, Inc.
Decision Date1987-03-11
Product CodeEJT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PONTALLOR 4 DENTAL ALLOY is the device name listed in this FDA 510(k) record. The listed applicant is Degussa Dental, Inc.. It received FDA 510(k) clearance on 1987-03-11 under 510(k) number K870024. The device is classified under product code EJT. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PONTALLOR 4 DENTAL ALLOY?

PONTALLOR 4 DENTAL ALLOY is a medical device that received FDA 510(k) clearance on 1987-03-11. The listed applicant is Degussa Dental, Inc.. The 510(k) number is K870024.

When did PONTALLOR 4 DENTAL ALLOY receive FDA 510(k) clearance?

PONTALLOR 4 DENTAL ALLOY received FDA 510(k) clearance on 1987-03-11, under 510(k) number K870024.

Who is the listed applicant for PONTALLOR 4 DENTAL ALLOY?

The FDA 510(k) record lists Degussa Dental, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PONTALLOR 4 DENTAL ALLOY?

The FDA product code for PONTALLOR 4 DENTAL ALLOY is EJT.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Degussa Dental, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K883758ALBABOND 60K883511ALBABOND EK883508HERA HK883509HERAEUS DG 63K883510DEGUPAL 4K883507HERAEUS C SPECIAL

View all 25 devices →

Related Devices (Code: EJT)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K052463PROMETAL HN86Prometal TechnologiesK041378BIO 60Kodent, Inc.K040672PORTA REFLEXWieland Dental + Technik GmbH & Co. KGK040524PORTA SOLDER 1090 WWieland Dental + Technik GmbH & Co. KGK040043NDX-40 ALLOYHeraeus Kulzer, Inc.K034049HERADOR EC, PF, C, H, NH, G, GG AND MP; HERALOY U AND G; HERABOND N; ALBABOND C, B AND A; BIO HERANORMHeraeus Kulzer,GmbH

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑