Medical Device Manufacturer · US , Walker , MI

Pacific Implant, Inc.

2 submissions · 2 cleared · Since 1981

Total

Cleared

Denied

Pacific Implant, Inc. — FDA 510(k) Submissions

Pacific Implant, Inc. has submitted 2 FDA 510(k) premarket notifications since 1981, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Implant, Endosseous, Root-form, Point, Silver, Endodontic . Use the specialty filter in the sidebar to narrow results.

2 devices

1–2 of 2

PACIFIC IMPLANT TITANIUM ENDODONTIC POINT

K992582 · EKL Point, Silver, Endodontic · Dental

Oct 1999 80d

INTRAOSSEOUS DENTAL IMPLANT

K813227 · DZE Implant, Endosseous,... · Dental

Dec 1981 51d

Data Source

FDA 510(k) public files . 174,402 total devices indexed.

Pacific Implant, Inc.

Pacific Implant, Inc. — FDA 510(k) Submissions

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