ClearanceBrief
Company ยท US

Loredan Biomedical, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1983 to 1993. Name variants (Inc, Corp, punctuation) are merged.

9510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
IKKSystem, Isokinetic Testing And Evaluation7
BXBExerciser, Powered1
LXJInteractive Rehabilitation Exercise Devices1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
May 12, 1993K924512LIDO V-TAK
Loredan Biomedical, Inc.
LXJ
Mar 31, 1993K924513LIDO(R) LINEA
Loredan Biomedical, Inc.
BXB
Aug 14, 1990K903429LIDO LINEA
Loredan Biomedical, Inc.
IKK
Nov 18, 1988K884487LIDO TM ACTIVE BACK
Loredan Biomedical, Inc.
IKK
Feb 26, 1988K880018LIDO(TM) WORKSET
Loredan Biomedical, Inc.
IKK
Feb 26, 1988K880017LIDO(TM) LIFT
Loredan Biomedical, Inc.
IKK
Jun 5, 1987K871793LIDO ACTIVE
Loredan Biomedical, Inc.
IKK
Jun 2, 1986K861986LIDO BACK
Loredan Biomedical, Inc.
IKK
Sep 26, 1983K832770LANE ONE
Loredan Biomedical, Inc.
IKK

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
Get alerts for these product codes