Company ยท US
Ostex Intl., Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1995 to 2001. Name variants (Inc, Corp, punctuation) are merged.
5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
| Code | Device | Records |
|---|---|---|
| JMM | Column Chromatography & Color Development, Hydroxyproline | 5 |
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Jul 30, 2001 | K011052 | OSTEOMARK NTX POINT OF CARE PRESCRIPTION HOME USE Ostex Intl., Inc. | JMM |
| Feb 2, 1999 | K983457 | OSTEOMARK NTX SERUM EIA Ostex Intl., Inc. | JMM |
| Mar 6, 1998 | K980518 | OSTEOMARK Ostex Intl., Inc. | JMM |
| Jul 11, 1996 | K961562 | OSTEOMARK Ostex Intl., Inc. | JMM |
| May 8, 1995 | K945946 | OSTEOMARK(R) Ostex Intl., Inc. | JMM |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||