FDA applicant
Look, Inc.
FDA records 25 decisions for Look, Inc. (Ada, OK) from 1987 to 1994: 25 510(k) clearances. Most are in product codes HMX (Cannula, Ophthalmic) and GAL (Suture, Absorbable, Natural). 1 recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Look, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Look, Inc. since 2007.
Recalls per year
1in 2011
Class I Class II/III not classified
Planning a device like Look, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) ReportOther applicant names beginning “Look”
FDA records each applicant name separately; these may or may not be the same firm.