Medical Device Manufacturer · US , Mchenry , IL

Spelna, Inc. - FDA 510(k) Cleared Devices

11 submissions · 11 cleared · Since 1982

Total

Cleared

Denied

Spelna, Inc. has 11 FDA 510(k) cleared dental devices. Based in Mchenry, US.

Historical record: 11 cleared submissions from 1982 to 1986.

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

Spelna, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Spelna, Inc.

11 devices

1-11 of 11

SATALEC SEPTOSONIC SC 80/SC 120

K852527 · FLG

General Hospital · 203d

5X2 SATALEC CHIROPODY CASE

K853200

General & Plastic Surgery · 126d

Cleared Jul 31, 1985

SATLEC PROPHY UNIT PU 3055

K852521 · KOJ

Dental · 47d

Cleared Jul 31, 1985

SATALEC SERVOTORQUE S2 SX2

K852524 · EIA

Dental · 47d

Cleared Mar 16, 1984

SATELEC SUPRASSON PIEZOMATIC P2

K832664 · ELC

Dental · 220d

Cleared Mar 16, 1984

SATELEC PROPHY UNIT PU 2000S

K832674 · ELC

Dental · 220d

Cleared Oct 19, 1983

SATELEC SUPRASSON SP 3055

K832665 · ELC

Dental · 71d

Cleared Oct 19, 1983

SATELEC PROPHY UNIT PU-2000

Cardiovascular · 147d

Spelna, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Spelna, Inc.

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