Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Acuity Polymers, Inc. — Predicate Candidate Screening

11 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

80 daysmedian FDA review time
148 days90th percentile
11clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K242393Acuity 181™ (tisilfocon A) and Acuity 181™ (tisilfocon A) wiAcuity Polymers, Inc.2024-11-01800
K240618Acuity 200™ (fluoroxyfocon A) Rigid Gas Permeable Contact LeAcuity Polymers, Inc.2024-04-03290
K230965Acuity 100™ (hexafocon A) with Tangible™ Hydra-PEG®, TYRO™-9Acuity Polymers, Inc.2023-06-16720
K213538Acuity 200 with Tangible Hydra-PEG (fluoroxyfocon A) Rigid GAcuity Polymers, Inc.2021-12-30520
K203571Acuity 200 (fluoroxyfocon A) Rigid Gas Permeable Contact LenAcuity Polymers, Inc.2021-04-091230
K201194Acuity 200™ (fluoroxyfocon A) Rigid Gas Permeable Contact LeAcuity Polymers, Inc.2020-09-081270
K180988Acuity 18 (enflufocon A) Rigid Gas Permeable Contact Lens, AAcuity Polymers, Inc.2018-06-08530
K170001Acuity 85 (Oprifocon A) Rigid Gas Permeable Contact LensAcuity Polymers, Inc.2017-06-021500
K170007Acuity 58 (Enflufocon B) Rigid Gas Permeable Contact LensAcuity Polymers, Inc.2017-05-311480
K163254Acuity 18 (enflufocon A) Rigid Gas Permeable Contact LensAcuity Polymers, Inc.2017-01-18580
K162005Acuity 100 (hexafocon A) Rigid Gas Permeable Contact LensAcuity Polymers, Inc.2016-12-081410

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda