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Sign in to claim this brandMED-MIZER, INC
US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 80 COMMERCE DRIVE, BATESVILLE, IN, 47006
- Website
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- —
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- Phone
- —
- PRRC Contact
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- EUDAMED SRN
- —
- FDA FEI Number
- 3004976058
- DUNS Number
- —
Catalogue (42)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Med-Mizer, Inc. | FF18-MAG | FDA UDI | Class I | Active |
| Med-Mizer, Inc. | FREEDOM FLEX 24 | FDA UDI | Class I | Active |
| Med-Mizer, Inc. | CC803 | FDA UDI | Class II | Unknown |
| Med-Mizer, Inc. | ACTIVECARE 36 ADJUST | FDA UDI | Class II | Active |
| Med-Mizer, Inc. | ALLCARE-C | FDA UDI | Class II | Active |
| Med-Mizer, Inc. | FREEDOM FLEX 16 | FDA UDI | Class I | Active |
| Med-Mizer, Inc. | MED-RISER MR600 | FDA UDI | Class I | Active |
| Med-Mizer, Inc. | PR1000 | FDA UDI | Class II | Unknown |
| Med-Mizer, Inc. | ACGOV BASIC | FDA UDI | Class II | Active |
| Med-Mizer, Inc. | PR8000 | FDA UDI | Class II | Unknown |
| Med-Mizer, Inc. | ACTIVECARE 36 DELUXE | FDA UDI | Class II | Active |
| Med-Mizer, Inc. | MED-RISER MR1000 | FDA UDI | Class I | Active |
| Med-Mizer, Inc. | PR8000DS | FDA UDI | Class II | Unknown |
| Med-Mizer, Inc. | ALLCARE | FDA UDI | Class II | Active |
| Med-Mizer, Inc. | RV6 | FDA UDI | Class II | Active |
| Med-Mizer, Inc. | ACTIVECARE 42 FIXED | FDA UDI | Class II | Active |
| Med-Mizer, Inc. | SS803 | FDA UDI | Class II | Unknown |
| Med-Mizer, Inc. | MedSurg | FDA UDI | Class II | Active |
| Med-Mizer, Inc. | FLEXTILT 24 | FDA UDI | Class I | Active |
| Med-Mizer, Inc. | MED-RISER MR450 | FDA UDI | Class I | Active |
| Med-Mizer, Inc. | FLEXTILT 20 | FDA UDI | Class I | Active |
| Med-Mizer, Inc. | SS763A | FDA UDI | Class II | Unknown |
| Med-Mizer, Inc. | RETRACT-F | FDA UDI | Class II | Active |
| Med-Mizer, Inc. | RETRACT-V | FDA UDI | Class II | Active |
| Med-Mizer, Inc. | SS803A | FDA UDI | Class II | Unknown |
| Med-Mizer, Inc. | FREEDOM FLEX 20 | FDA UDI | Class I | Active |
| Med-Mizer, Inc. | EX6000 | FDA UDI | Class II | Unknown |
| Med-Mizer, Inc. | MED-RISER STS500 | FDA UDI | Class I | Active |
| Med-Mizer, Inc. | EX8000LC | FDA UDI | Class II | Active |
| Med-Mizer, Inc. | ACTIVECARE 42 ADJUST | FDA UDI | Class II | Active |
| Med-Mizer, Inc. | EX8000 | FDA UDI | Class II | Active |
| Med-Mizer, Inc. | M450 | FDA UDI | Class I | Active |
| Med-Mizer, Inc. | ACTIVECARE 42 DELUXE | FDA UDI | Class II | Active |
| Med-Mizer, Inc. | ET450 | FDA UDI | Class I | Active |
| Med-Mizer, Inc. | FLEXTILT 16 | FDA UDI | Class I | Active |
| Med-Mizer, Inc. | SELECTCARE | FDA UDI | Class II | Active |
| Med-Mizer, Inc. | EX5000C | FDA UDI | Class II | Unknown |
| Med-Mizer, Inc. | ACTIVECARE 36 FIXED | FDA UDI | Class II | Active |
| Med-Mizer, Inc. | ACGOV ADVANCED | FDA UDI | Class II | Active |
| Med-Mizer, Inc. | EX5000A | FDA UDI | Class II | Unknown |
| Med-Mizer, Inc. | PR1000DS | FDA UDI | Class II | Unknown |
| Med-Mizer, Inc. | SS763 | FDA UDI | Class II | Unknown |
Related Companies
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FDA Recalls (6)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Feb 3, 2023 | Z-1205-2023 | — | open, classified | Risk of boom pivot failing due to the nut securing the boom becoming loose and the bolt to be unsecure to the flange on the side. |
| Feb 3, 2023 | Z-1204-2023 | — | open, classified | Risk of boom pivot failing due to the nut securing the boom becoming loose and the bolt to be unsecure to the flange on the side. |
| Jul 25, 2018 | Z-3183-2018 | — | terminated | Under certain conditions, when pivoting bed to the extreme left there are situations where the wire/cables may become pinched. A failure would result in the resident requiring to be transferred to a different bed until repairs can be made |
| Apr 18, 2014 | Z-1541-2014 | — | terminated | All configurations of the SS Retractabed, Clinical Contour, made prior to June 7 2008 may have had insufficient welding on the foot cross tube. This tube is responsible for holding the two support rails together when using the foot side rails and keeps them from separating from the frame. If the weld on the tube breaks, it can lead to bed collapse or the rollers coming out of the channel on th |
| Apr 18, 2014 | Z-1542-2014 | — | terminated | All configurations of the SS Retractabed, Clinical Contour, made prior to June 7 2008 may have had insufficient welding on the foot cross tube. This tube is responsible for holding the two support rails together when using the foot side rails and keeps them from separating from the frame. If the weld on the tube breaks, it can lead to bed collapse or the rollers coming out of the channel on th |
| Apr 18, 2014 | Z-1543-2014 | — | terminated | All configurations of the SS Retractabed, Clinical Contour, made prior to June 7, 2008 may have had insufficient welding on the foot cross tube. This tube is responsible for holding the two support rails together when using the foot side rails and keeps them from separating from the frame. If the weld on the tube breaks, it can lead to bed collapse or the rollers coming out of the channel on t |