Medical Device Manufacturer · US , Mchenry , IL

Geistlich-Pharma - FDA 510(k) Cleared Devices

16 submissions · 15 cleared · Since 1983

Recent clearances: BIO-OSS, BIO-OSS BLOCKS AND BIO-OSS COLLAGEN, ORTHOSS RESORBABLE BONE VOID FILLER, BIO-BLOCKS

Total

Cleared

Denied

Geistlich-Pharma has 15 FDA 510(k) cleared dental devices. Based in Mchenry, US.

Historical record: 15 cleared submissions from 1983 to 2004.

Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.

Geistlich-Pharma is one of 5868 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Geistlich-Pharma

16 devices

1-12 of 16

Cleared Jan 15, 2004

BIO-OSS, BIO-OSS BLOCKS AND BIO-OSS COLLAGEN

K033815 · NPM

Dental · 37d

Cleared Mar 28, 2002

ORTHOSS RESORBABLE BONE VOID FILLER

BIO-OSS ANORGANIC BOVINE BONE

K970321 · LYC

Dental · 595d

Cleared Jul 24, 1998

RESOR-PIN RESORBABLE MEMBRANE PIN

K972817 · LYC

Dental · 360d

Cleared Jun 11, 1997

BIO-GIDE RESORBABLE BILAYER MEMBRANE

SONAR-AID(R) ULTRASOUND STANDOFF PAD

K874943 · ITX

Radiology · 236d

Geistlich-Pharma - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Geistlich-Pharma

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