Aladan Corp.
Jessup, MD, US
Aladan Corp. appears in FDA device records in Jessup, MD. FDA records list 18 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 18
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 18 510(k) clearances for Aladan Corp. between 1989 and 1996. The busiest year on record is 1995, with 5. The most recent is 1996, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1989 | 2 |
| 1990 | 4 |
| 1991 | 4 |
| 1994 | 2 |
| 1995 | 5 |
| 1996 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K960590 | TRI-CLEAN 110/TRI-CLEAN PLUS GLOVE | LYY | Substantially Equivalent | |
| K952404 | SAFETEX SUPER HYPERALLERGENIC POWDERFREE LATEX MEDICAL GLOVE | LYY | Substantially Equivalent | |
| K952556 | SAFETEX SUPER HYPOALLERGENIC POWDERED LATEX EXAMINATION GLOVE | LYY | Substantially Equivalent | |
| K943933 | SAXON GOLD ULTRA SPERMICIDAL RAINBOW CONDOM | HIS | Substantially Equivalent | |
| K951839 | ALADAN HYPOALLERGENIC LATEX MEDICAL EXAMINATION GLOVES | LYY | Substantially Equivalent | |
| K943883 | SAXON GOLD ULTRA SPERMICIDAL RAINBOW CONDOM | HIS | Substantially Equivalent | |
| K942758 | HYPOALLERGEN NON-STER POWDERFREE LATEX PAT EXAM GLOVE | LYY | Substantially Equivalent | |
| K940873 | SAFETEX HYPOALLERGENIC POWDERFREE LATEX EXAMINATION GLOVE | LYY | Substantially Equivalent | |
| K911774 | ALADAN LATEX MEDICAL GLOVE | LYY | Substantially Equivalent | |
| K911447 | LATEX EXAMINATION GLOVES (HYPOALLERGENIC) | LYY | Substantially Equivalent | |
| K905279 | CONDOM (RUBBER) CONTRACEPTIVE | HIS | Substantially Equivalent | |
| K905678 | ALADERM | LYY | Substantially Equivalent | |
| K902565 | ALADAN TRI-CLEAN 110 POWDERLESS LATEX GLOVE | LYY | Substantially Equivalent | |
| K901416 | CONDOM (RUBBER) CONTRACEPTIVE | HIS | Substantially Equivalent | |
| K902182 | MODIFIED STERILE LATEX EXAMINATION GLOVES | LYY | Substantially Equivalent | |
| K902181 | MODIFIED NON-STERILE LATEX EXAMINATION GLOVES | LYY | Substantially Equivalent | |
| K890880 | ALADAN STERILE LATEX MEDICAL GLOVE | LYY | Substantially Equivalent | |
| K890627 | UNSTERILE PATIENT EXAMINATION GLOVE | LYY | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain