# Ace Orthopedic Manufacturing Co.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 14 (1977–1994): 14 510(k) clearances
- Product codes: JEC (5), HSB (2), HAX (1), KOA (1), HXK (1), KTT (1), JDW (1), HWC (1), HRS (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 15 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- DePuy Orthopaedics, Inc.: 6 (https://510kreport.com/company/depuy-orthopaedics)
- Biomet, Inc.: 3 (https://510kreport.com/company/biomet)
- Merete Medical GmbH: 1 (https://510kreport.com/company/merete-medical)
- Biomet Orthopedics, Inc.: 1 (https://510kreport.com/company/biomet-orthopedics)
- Smith & Nephew, Inc.: 1 (https://510kreport.com/company/smith-nephew)
- Depuy Ace: 1 (https://510kreport.com/company/depuy-ace)
- Depuy Ace Medical Co.: 1 (https://510kreport.com/company/depuy-ace-medical)
- Orthohelix Surgical Designs, Inc.: 1 (https://510kreport.com/company/orthohelix-surgical-designs)

## Its most-cited devices
- K813554: Ace/Kyle Captured Hip Screw (1982), cited by 5
- K920738: Ace 100 Degrees Tubular Plate (1992), cited by 3
- K934643: Ace Humeral Nail (1994), cited by 2
- K926047: Ace 8.0MM Cannulated Cancellous Bone Screw (1993), cited by 2
- K810193: Trippi-Wells Dual Purpose Universal Tong (1981), cited by 1
- K801594: Ace Fischer External Fixation Device (1980), cited by 1

## Recent decisions
- K934643: Ace Humeral Nail (Mar 22, 1994)
- K934962: Aim Supracondylar Nail (Mar 22, 1994)
- K936045: Ace Unilateral Fixator II (Feb 22, 1994)
- K926047: Ace 8.0MM Cannulated Cancellous Bone Screw (Mar 31, 1993)
- K920738: Ace 100 Degrees Tubular Plate (Jul 27, 1992)
- K813554: Ace/Kyle Captured Hip Screw (Jan 12, 1982)
- K810193: Trippi-Wells Dual Purpose Universal Tong (Mar 20, 1981)
- K801594: Ace Fischer External Fixation Device (Sep 9, 1980)

Source page: https://510kreport.com/company/ace-orthopedic-manufacturing