K954094Substantially Equivalent
Ophta Sil- Punctal Plugs (Modification)
G.W.B. Intl., Ltd., Marshfield MA / Traditional, Substantially Equivalent
K954094 is the FDA 510(k) clearance record for OPHTA SIL- PUNCTAL PLUGS (MODIFICATION), cleared for G.W.B. Intl., Ltd. on under FDA product code LZU (Plug, Punctum). FDA records list 8 510(k) clearances for G.W.B. Intl., Ltd., from to . As of , FDA records show no recalls naming K954094.
Clearance record
- Decision date
- Received
- (42 days to decision)
- Product code
- LZU Plug, Punctum
- Device class
- Unclassified
- Review panel
- Unknown
- Applicant
- G.W.B. Intl., Ltd. P.O. Box 465, Marshfield MA
- 510(k) summary
- Statement
- Third party review
- No
Clearances, product code LZU
Trailing 12 monthsFDA records hold no clearances under product code LZU in the trailing twelve months.
Show the numbers
| Month | Clearances |
|---|---|
| November 2025 | 0 |
| December 2025 | 0 |
| January 2026 | 0 |
| February 2026 | 0 |
| March 2026 | 0 |
| April 2026 | 0 |
| May 2026 | 0 |
| June 2026 | 0 |
| July 2026 | 0 |
| August 2026 | 0 |
| September 2026 | 0 |
| October 2026 | 0 |
FIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.
