Medical Device Manufacturer · US , San Leandro , CA

Berkeley Advanced Biomaterials, Inc. - FDA 510(k) Cleared Devices

13 submissions · 13 cleared · Since 2003

Total

Cleared

Denied

Berkeley Advanced Biomaterials, Inc. has 13 FDA 510(k) cleared orthopedic devices. Based in San Leandro, US.

Historical record: 13 cleared submissions from 2003 to 2012.

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

FDA 510(k) Regulatory Record - Berkeley Advanced Biomaterials, Inc.

13 devices

1-13 of 13

BI-OSTETIC FOAM AND PUTTY, GENEROS FOAM AND PUTTY

K092046 · MQV

Orthopedic · 261d

Cleared Jul 06, 2006

BI-OSTETIC FOAM, CEM-OSTETIC FOAM, TRI-OSTETIC FOAM, GENEROS FOAM

K053213 · MQV

Orthopedic · 232d

Cleared Nov 03, 2005

GENEROS 80, GENEROS 60

GENEROS, MODELS GO-01G, GO-05G, GO-10G, GO-15G, GO-20G, GO-30G, GO-40G,...

CEM-OSTETIC PUTTY INJECTION KIT, MODEL PIK-XX, PIK-XX-YY

CEM-OSTETIC, MODELS CEMO-020O, CEMO-05P, CEMO-10P, CEMO-20P, AND CEMO-30P

K022622 · MQV

Orthopedic · 155d

Berkeley Advanced Biomaterials, Inc. - FDA 510(k) Cleared Devices

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