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FDA 510(k)

MATCHMAKER/PROPAQUE PORCELAIN

K-Number: K960770 · 1996-11-19

ApplicantDavis Schottlander & Davis, Ltd.
Decision Date1996-11-19
Product CodeELL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MATCHMAKER/PROPAQUE PORCELAIN is the device name listed in this FDA 510(k) record. The listed applicant is Davis Schottlander & Davis, Ltd.. It received FDA 510(k) clearance on 1996-11-19 under 510(k) number K960770. The device is classified under product code ELL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MATCHMAKER/PROPAQUE PORCELAIN?

MATCHMAKER/PROPAQUE PORCELAIN is a medical device that received FDA 510(k) clearance on 1996-11-19. The listed applicant is Davis Schottlander & Davis, Ltd.. The 510(k) number is K960770.

When did MATCHMAKER/PROPAQUE PORCELAIN receive FDA 510(k) clearance?

MATCHMAKER/PROPAQUE PORCELAIN received FDA 510(k) clearance on 1996-11-19, under 510(k) number K960770.

Who is the listed applicant for MATCHMAKER/PROPAQUE PORCELAIN?

The FDA 510(k) record lists Davis Schottlander & Davis, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MATCHMAKER/PROPAQUE PORCELAIN?

The FDA product code for MATCHMAKER/PROPAQUE PORCELAIN is ELL.

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Other records listing Davis Schottlander & Davis, Ltd. 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.

K024252MATCH MASTER LOW FUSION PORCELAINK024250MATCH PRESS PRESSABLE CERAMICK001463SCHOTTLANDER ENIGMA COLOUR TONE, MODEL 0156K993717ENIGMA HI-BASE DENTURE BASE MATERIALK984134NATURA DENTURE TEETHK984128ENIGMA DENTURE TEETH

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Related Devices (Code: ELL)

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.

K240586Additive Manufacturing Zirconia Customized RestorationHangzhou Thales Medtech Co., Ltd.K203072Franz Zirconia Dental CrownFranz Biotech, Inc.K162043NobelProcera HT ML FCZ BridgeNobel Biocare ABK153534NobelProcera HT ML Full Contour Zirconia CrownNobel Biocare ABK071182PROCERA BRIDGE ZIRCONIA 9 UNITS-14 UNITS, MODELS 30-4004 TO 30-4013Nobel Biocare ABK060530SD CERAMIC COPING FOR QUICK ABUTMENT, LOCKING. MODEL 45301. RD CERAMIC COPING FOR QUICK ABUTMENT, LOCKING, MODEL 45302.Lifecore Biomedical, Inc.

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.

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