GEISTLICH BIO-OSS PEN (0.25 G, 0.25-1.0MM GRANULES), GEISTLICH BIO-OSS PEN (0.5 G, 0.25-1.0MM GRANULES), GEISTLICH BIO-O— 510(k) K120601

Substantially Equivalent

Geistlich Pharma AG

FDA 510(k) clearance K120601 for GEISTLICH BIO-OSS PEN (0.25 G, 0.25-1.0MM GRANULES), GEISTLICH BIO-OSS PEN (0.5 G, 0.25-1.0MM GRANULES), GEISTLICH BIO-O, Substantially Equivalent on 2012-05-24. Applicant: Geistlich Pharma AG. Device class: 2.

Clearance details

Applicant
Geistlich Pharma AG
Product code
Code NPM
Device class
Class 2
Regulation
21 CFR 872.3930
Advisory panel
Dental
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Washington, DC, US
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Recalls naming K120601

K-number listed on FDA's recall record

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K120601.

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