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Lic-Orthion

FDA Regulatory Profile

Lic-Orthion has 0 FDA recalls, 0 inspections, 17 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Apr 4, 1989

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances17Oct 4, 2026Not statedCurrent
Inspections0Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent 510(k) Clearances

K-NumberDeviceDate
K891649PATIENT EXAMINATION GLOVES (LATEX)Apr 4, 1989
K862022LIC-ORTHION MULTI-THERAPY TREATMENT TABLEJun 19, 1986
K854729ADAM (ABSORBENT INCONTINENCE SHIELD)Feb 6, 1986
K854730DAISY (ABSORBENT INCONTINENCE SHIELD)Feb 6, 1986
K851471TRIBAG, TRIBAND & TRIFIX-REUSEABLE URINE COLLECTORJun 12, 1985
K851470BIBAG, BIBAND & BIFIX - SINGLE USE URINE COLLECTORJun 12, 1985
K843234CITOMAT AUTOCLAVESOct 25, 1984
K843233ANATOM SYSTEMOct 25, 1984
K830853LAVATORY SEAT HEIGHTENERJun 8, 1983
K830849OB TILTApr 5, 1983
K830848RESI-WALKERApr 5, 1983
K830854COLLAPSABLE LAVATORY SEAT HEIGHTENERApr 5, 1983
K830852SHOWER STOOL W/HANDLESApr 5, 1983
K830850OB TRIPP TRANSPORT CHAIRApr 5, 1983
K830851BATH TUB SEAT & BATH BOARDApr 5, 1983
K830855SESAM TREATMENT TABLEApr 5, 1983
K830842OB HELP ARMApr 5, 1983

FDA data resources